Canonical Allele Identifier: CA359781012

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171021G>C (hg19) ; chr5:g.56875194G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875194G>C , CM000667.2:g.56875194G>C	GRCh38
NC_000005.9:g.56171021G>C , CM000667.1:g.56171021G>C	GRCh37
NC_000005.8:g.56206778G>C	NCBI36
NG_031884.1:g.65122G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1849G>C MANE Select	ENSP00000382423.3:p.Gly617Arg
ENST00000399503.3:c.1849G>C	ENSP00000382423.3:p.Gly617Arg
NM_005921.1:c.1849G>C	NP_005912.1:p.Gly617Arg
XM_005248519.3:c.1471G>C	XP_005248576.2:p.Gly491Arg
XM_011543406.1:c.1594G>C	XP_011541708.1:p.Gly532Arg
XM_011543407.1:c.1686+2189G>C	XP_011541709.1:n.1686+2189G>C
XM_011543408.1:c.1849G>C	XP_011541710.1:p.Gly617Arg
XM_017009484.1:c.1438G>C	XP_016864973.1:p.Gly480Arg
XM_017009485.1:c.1360G>C	XP_016864974.1:p.Gly454Arg
XR_001742068.2:n.1880G>C
NM_005921.2:c.1849G>C MANE Select	NP_005912.1:p.Gly617Arg