Canonical Allele Identifier: CA359802573

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155669G>C (hg19) ; chr5:g.56859842G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859842G>C , CM000667.2:g.56859842G>C	GRCh38
NC_000005.9:g.56155669G>C , CM000667.1:g.56155669G>C	GRCh37
NC_000005.8:g.56191426G>C	NCBI36
NG_031884.1:g.49770G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.761G>C MANE Select	ENSP00000382423.3:p.Gly254Ala
ENST00000399503.3:c.761G>C	ENSP00000382423.3:p.Gly254Ala
NM_005921.1:c.761G>C	NP_005912.1:p.Gly254Ala
XM_005248519.3:c.383G>C	XP_005248576.2:p.Gly128Ala
XM_011543406.1:c.506G>C	XP_011541708.1:p.Gly169Ala
XM_011543407.1:c.761G>C	XP_011541709.1:p.Gly254Ala
XM_011543408.1:c.761G>C	XP_011541710.1:p.Gly254Ala
XM_017009484.1:c.350G>C	XP_016864973.1:p.Gly117Ala
XM_017009485.1:c.272G>C	XP_016864974.1:p.Gly91Ala
XR_001742068.2:n.792G>C
NM_005921.2:c.761G>C MANE Select	NP_005912.1:p.Gly254Ala