Canonical Allele Identifier: CA454723966

Gene: CDK13

Linked Data

• MyVariant Identifiers: chr7:g.40038972T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.39999373T>C , CM000669.2:g.39999373T>C	GRCh38
NC_000007.13:g.40038972T>C , CM000669.1:g.40038972T>C	GRCh37
NC_000007.12:g.40005497T>C	NCBI36
NG_052965.1:g.54014T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000181839.10:c.2055T>C MANE Select	ENSP00000181839.4:p.Pro685=
ENST00000340829.10:c.2055T>C	ENSP00000340557.5:p.Pro685=
ENST00000484589.2:c.607T>C
ENST00000642213.1:n.537T>C
ENST00000642660.1:n.935T>C
ENST00000643859.1:c.946T>C
ENST00000643915.1:c.369T>C	ENSP00000496187.1:p.Pro123=
ENST00000646039.1:c.1395T>C	ENSP00000494168.1:p.Pro465=
ENST00000646437.1:c.689T>C
ENST00000647453.1:n.1124T>C
ENST00000647518.1:n.3892T>C
ENST00000181839.8:c.2055T>C	ENSP00000181839.4:p.Pro685=
ENST00000340829.9:c.2055T>C	ENSP00000340557.5:p.Pro685=
ENST00000484589.1:n.607T>C
ENST00000611390.1:c.213T>C	ENSP00000484610.1:p.Pro71=
ENST00000613626.4:c.213T>C	ENSP00000480835.1:p.Pro71=
NM_003718.4:c.2055T>C	NP_003709.3:p.Pro685=
NM_031267.3:c.2055T>C	NP_112557.2:p.Pro685=
XM_011515597.1:c.2055T>C	XP_011513899.1:p.Pro685=
XM_011515598.1:c.2055T>C	XP_011513900.1:p.Pro685=
XM_011515597.3:c.2055T>C	XP_011513899.1:p.Pro685=
XM_017012750.2:c.2055T>C	XP_016868239.1:p.Pro685=
XM_017012751.2:c.2055T>C	XP_016868240.1:p.Pro685=
NM_003718.5:c.2055T>C MANE Select	NP_003709.3:p.Pro685=