Canonical Allele Identifier: CA2012239234

Gene: CACNA1C DCP1B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1988550T>G , CM000674.2:g.1988550T>G	GRCh38
NC_000012.11:g.2097716T>G , CM000674.1:g.2097716T>G	GRCh37
NC_000012.10:g.1967977T>G	NCBI36
NG_008801.2:g.22765T>G , LRG_334:g.22765T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682462.1:c.139+17349T>G (CACNA1C)	ENSP00000507105.1:n.139+17349T>G
ENST00000682544.1:c.139+17349T>G (CACNA1C)	ENSP00000507184.1:n.139+17349T>G
ENST00000683781.1:c.139+17349T>G (CACNA1C)	ENSP00000507434.1:n.139+17349T>G
ENST00000683824.1:c.139+17349T>G (CACNA1C)	ENSP00000507867.1:n.139+17349T>G
ENST00000683840.1:c.139+17349T>G (CACNA1C)	ENSP00000507612.1:n.139+17349T>G
ENST00000683956.1:c.139+17349T>G (CACNA1C)	ENSP00000506882.1:n.139+17349T>G
ENST00000280665.11:c.319+4714A>C (DCP1B) MANE Select	ENSP00000280665.6:n.319+4714A>C
ENST00000280665.10:c.319+4714A>C (DCP1B)	ENSP00000280665.6:n.319+4714A>C
ENST00000537725.1:n.315+4714A>C (DCP1B)
ENST00000541700.5:n.436+4714A>C (DCP1B)
ENST00000543114.1:c.139+17349T>G (CACNA1C)	ENSP00000445849.1:n.139+17349T>G
ENST00000543381.5:c.*85+2571A>C (DCP1B)	ENSP00000445011.1:n.*85+2571A>C
NM_152640.3:c.319+4714A>C (DCP1B)	NP_689853.3:n.319+4714A>C
XM_006719017.1:c.139+17349T>G (CACNA1C)	XP_006719080.1:n.139+17349T>G
XM_011520927.1:c.13+2571A>C (DCP1B)	XP_011519229.1:n.13+2571A>C
XM_011520928.1:c.-63+3494A>C (DCP1B)	XP_011519230.1:n.-63+3494A>C
XM_011521020.1:c.139+17349T>G (CACNA1C)	XP_011519322.1:n.139+17349T>G
NM_152640.4:c.319+4714A>C (DCP1B)	NP_689853.3:n.319+4714A>C
NR_135060.1:n.549+2571A>C (DCP1B)
XM_006719017.2:c.139+17349T>G (CACNA1C)	XP_006719080.1:n.139+17349T>G
XM_011520927.3:c.13+2571A>C (DCP1B)	XP_011519229.1:n.13+2571A>C
XM_011521020.2:c.139+17349T>G (CACNA1C)	XP_011519322.1:n.139+17349T>G
XM_017019926.2:c.139+17349T>G (CACNA1C)	XP_016875415.1:n.139+17349T>G
XM_017019927.2:c.139+17349T>G (CACNA1C)	XP_016875416.1:n.139+17349T>G
XM_017019928.2:c.139+17349T>G (CACNA1C)	XP_016875417.1:n.139+17349T>G
XM_017019929.2:c.139+17349T>G (CACNA1C)	XP_016875418.1:n.139+17349T>G
XM_017019930.2:c.139+17349T>G (CACNA1C)	XP_016875419.1:n.139+17349T>G
XM_017019931.2:c.139+17349T>G (CACNA1C)	XP_016875420.1:n.139+17349T>G
XM_017019932.2:c.139+17349T>G (CACNA1C)	XP_016875421.1:n.139+17349T>G
XM_017019933.2:c.139+17349T>G (CACNA1C)	XP_016875422.1:n.139+17349T>G
XM_017019934.2:c.139+17349T>G (CACNA1C)	XP_016875423.1:n.139+17349T>G
XM_017019935.2:c.139+17349T>G (CACNA1C)	XP_016875424.1:n.139+17349T>G
XM_017019936.2:c.139+17349T>G (CACNA1C)	XP_016875425.1:n.139+17349T>G
XM_017019937.2:c.139+17349T>G (CACNA1C)	XP_016875426.1:n.139+17349T>G
XM_017019938.2:c.139+17349T>G (CACNA1C)	XP_016875427.1:n.139+17349T>G
XM_017019939.2:c.139+17349T>G (CACNA1C)	XP_016875428.1:n.139+17349T>G
XM_017019940.2:c.139+17349T>G (CACNA1C)	XP_016875429.1:n.139+17349T>G
XM_017019941.2:c.139+17349T>G (CACNA1C)	XP_016875430.1:n.139+17349T>G
XM_017019942.2:c.139+17349T>G (CACNA1C)	XP_016875431.1:n.139+17349T>G
XM_017019943.2:c.139+17349T>G (CACNA1C)	XP_016875432.1:n.139+17349T>G
XM_017019944.2:c.139+17349T>G (CACNA1C)	XP_016875433.1:n.139+17349T>G
XM_017019945.2:c.139+17349T>G (CACNA1C)	XP_016875434.1:n.139+17349T>G
XM_017019946.2:c.139+17349T>G (CACNA1C)	XP_016875435.1:n.139+17349T>G
XM_017019947.2:c.139+17349T>G (CACNA1C)	XP_016875436.1:n.139+17349T>G
XM_017019948.2:c.139+17349T>G (CACNA1C)	XP_016875437.1:n.139+17349T>G
XM_017019949.2:c.139+17349T>G (CACNA1C)	XP_016875438.1:n.139+17349T>G
XM_017019950.2:c.139+17349T>G (CACNA1C)	XP_016875439.1:n.139+17349T>G
XM_017019951.2:c.139+17349T>G (CACNA1C)	XP_016875440.1:n.139+17349T>G
XM_017019952.2:c.139+17349T>G (CACNA1C)	XP_016875441.1:n.139+17349T>G
XM_017019953.1:c.139+17349T>G (CACNA1C)	XP_016875442.1:n.139+17349T>G
XM_017019954.1:c.139+17349T>G (CACNA1C)	XP_016875443.1:n.139+17349T>G
XM_017019955.2:c.139+17349T>G (CACNA1C)	XP_016875444.1:n.139+17349T>G
NM_152640.5:c.319+4714A>C (DCP1B) MANE Select	NP_689853.3:n.319+4714A>C
NR_135060.2:n.471+2571A>C (DCP1B)