Canonical Allele Identifier: CA359786171

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177640G>C (hg19) ; chr5:g.56881813G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881813G>C , CM000667.2:g.56881813G>C	GRCh38
NC_000005.9:g.56177640G>C , CM000667.1:g.56177640G>C	GRCh37
NC_000005.8:g.56213397G>C	NCBI36
NG_031884.1:g.71741G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2613G>C MANE Select	ENSP00000382423.3:p.Leu871Phe
ENST00000399503.3:c.2613G>C	ENSP00000382423.3:p.Leu871Phe
NM_005921.1:c.2613G>C	NP_005912.1:p.Leu871Phe
XM_005248519.3:c.2235G>C	XP_005248576.2:p.Leu745Phe
XM_011543406.1:c.2358G>C	XP_011541708.1:p.Leu786Phe
XM_011543407.1:c.2334G>C	XP_011541709.1:p.Leu778Phe
XM_011543408.1:c.2613G>C	XP_011541710.1:p.Leu871Phe
XM_017009484.1:c.2202G>C	XP_016864973.1:p.Leu734Phe
XM_017009485.1:c.2124G>C	XP_016864974.1:p.Leu708Phe
XR_001742068.2:n.2644G>C
NM_005921.2:c.2613G>C MANE Select	NP_005912.1:p.Leu871Phe