Canonical Allele Identifier: CA367288961

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40041459G>C (hg19) ; chr7:g.40001860G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.40001860G>C , CM000669.2:g.40001860G>C	GRCh38
NC_000007.13:g.40041459G>C , CM000669.1:g.40041459G>C	GRCh37
NC_000007.12:g.40007984G>C	NCBI36
NG_052965.1:g.56501G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2183-1G>C MANE Select	ENSP00000181839.4:n.2183-1G>C
ENST00000340829.10:c.2183-1G>C	ENSP00000340557.5:n.2183-1G>C
ENST00000484589.2:c.735-1G>C
ENST00000642213.1:n.665-1G>C
ENST00000643859.1:c.1074-1G>C
ENST00000643915.1:c.497-1G>C	ENSP00000496187.1:n.497-1G>C
ENST00000645470.1:c.113-1G>C	ENSP00000495036.1:n.113-1G>C
ENST00000646039.1:c.1523-1G>C	ENSP00000494168.1:n.1523-1G>C
ENST00000647453.1:n.1252-1G>C
ENST00000647518.1:n.4020-1G>C
ENST00000181839.8:c.2183-1G>C	ENSP00000181839.4:n.2183-1G>C
ENST00000340829.9:c.2183-1G>C	ENSP00000340557.5:n.2183-1G>C
ENST00000484589.1:n.735-1G>C
ENST00000611390.1:c.341-1G>C	ENSP00000484610.1:n.341-1G>C
ENST00000613626.4:c.341-1G>C	ENSP00000480835.1:n.341-1G>C
NM_003718.4:c.2183-1G>C	NP_003709.3:n.2183-1G>C
NM_031267.3:c.2183-1G>C	NP_112557.2:n.2183-1G>C
XM_011515597.1:c.2183-1G>C	XP_011513899.1:n.2183-1G>C
XM_011515598.1:c.2183-1G>C	XP_011513900.1:n.2183-1G>C
XM_011515597.3:c.2183-1G>C	XP_011513899.1:n.2183-1G>C
XM_017012750.2:c.2183-1G>C	XP_016868239.1:n.2183-1G>C
XM_017012751.2:c.2183-1G>C	XP_016868240.1:n.2183-1G>C
NM_003718.5:c.2183-1G>C MANE Select	NP_003709.3:n.2183-1G>C