Canonical Allele Identifier: CA13719300
Gene: CACNA1C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10848632

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.2206827C>T , CM000674.2:g.2206827C>T GRCh38
NC_000012.10:g.2186254C>T NCBI36
NC_000012.11:g.2315993C>T , CM000674.1:g.2315993C>T GRCh37
NG_008801.2:g.241042C>T , LRG_334:g.241042C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327702.11:n.477+86397C>T ENSP00000329877.7:p.=
ENST00000335762.9:c.477+86397C>T ENSP00000336982.5:p.=
ENST00000344100.7:n.477+86397C>T ENSP00000341092.3:p.=
ENST00000347598.8:n.477+86397C>T ENSP00000266376.6:p.=
ENST00000399591.5:n.477+86397C>T ENSP00000382500.1:p.=
ENST00000399595.5:n.477+86397C>T ENSP00000382504.1:p.=
ENST00000399597.5:n.477+86397C>T ENSP00000382506.1:p.=
ENST00000399601.5:n.477+86397C>T ENSP00000382510.1:p.=
ENST00000399603.5:n.477+86397C>T ENSP00000382512.1:p.=
ENST00000399606.5:n.477+86397C>T ENSP00000382515.1:p.=
ENST00000399617.5:n.477+86397C>T ENSP00000382526.1:p.=
ENST00000399621.5:n.477+86397C>T ENSP00000382530.1:p.=
ENST00000399629.5:n.477+86397C>T ENSP00000382537.1:p.=
ENST00000399634.5:n.477+86397C>T ENSP00000382542.1:p.=
ENST00000399637.5:n.477+86397C>T ENSP00000382546.1:p.=
ENST00000399638.5:n.477+86397C>T ENSP00000382547.1:p.=
ENST00000399641.5:n.477+86397C>T ENSP00000382549.1:p.=
ENST00000399644.5:n.477+86397C>T ENSP00000382552.1:p.=
ENST00000399649.5:n.477+86397C>T ENSP00000382557.1:p.=
ENST00000399655.5:c.477+86397C>T ENSP00000382563.1:p.=
ENST00000402845.7:n.477+86397C>T ENSP00000385724.3:p.=
ENST00000406454.7:n.477+86397C>T ENSP00000385896.3:p.=
ENST00000480911.5:c.477+86397C>T ENSP00000437936.1:p.=
NM_000719.6:c.477+86397C>T , LRG_334t1:c.477+86397C>T NP_000710.5:p.=
NM_001129827.1:c.477+86397C>T , LRG_334t2:c.477+86397C>T NP_001123299.1:p.=
NM_001129829.1:c.477+86397C>T VV NP_001123301.1:p.=
NM_001129830.2:c.477+86397C>T VV NP_001123302.2:p.=
NM_001129831.1:c.477+86397C>T VV NP_001123303.1:p.=
NM_001129832.1:c.477+86397C>T VV NP_001123304.1:p.=
NM_001129833.1:c.477+86397C>T VV NP_001123305.1:p.=
NM_001129834.1:c.477+86397C>T VV NP_001123306.1:p.=
NM_001129835.1:c.477+86397C>T VV NP_001123307.1:p.=
NM_001129836.1:c.477+86397C>T VV NP_001123308.1:p.=
NM_001129837.1:c.477+86397C>T VV NP_001123309.1:p.=
NM_001129838.1:c.477+86397C>T VV NP_001123310.1:p.=
NM_001129839.1:c.477+86397C>T VV NP_001123311.1:p.=
NM_001129840.1:c.477+86397C>T , LRG_334t4:c.477+86397C>T NP_001123312.1:p.=
NM_001129841.1:c.477+86397C>T VV NP_001123313.1:p.=
NM_001129842.1:c.477+86397C>T VV NP_001123314.1:p.=
NM_001129843.1:c.477+86397C>T VV NP_001123315.1:p.=
NM_001129844.1:c.477+86397C>T VV NP_001123316.1:p.=
NM_001129846.1:c.477+86397C>T VV NP_001123318.1:p.=
NM_001167623.1:c.477+86397C>T VV NP_001161095.1:p.=
NM_001167624.2:c.477+86397C>T VV NP_001161096.2:p.=
NM_001167625.1:c.477+86397C>T VV NP_001161097.1:p.=
NM_199460.3:c.477+86397C>T VV NP_955630.3:p.=
XM_006719017.1:c.567+86397C>T XP_006719080.1:p.=
XM_011521018.1:c.-642+86397C>T XP_011519320.1:p.=
XM_011521020.1:c.567+86397C>T XP_011519322.1:p.=
XM_011521021.1:c.477+86397C>T XP_011519323.1:p.=
XM_011521022.1:c.477+86397C>T XP_011519324.1:p.=
XM_011521023.1:c.477+86397C>T XP_011519325.1:p.=