Canonical Allele Identifier: CA359781064

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171033G>C (hg19) ; chr5:g.56875206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875206G>C , CM000667.2:g.56875206G>C	GRCh38
NC_000005.9:g.56171033G>C , CM000667.1:g.56171033G>C	GRCh37
NC_000005.8:g.56206790G>C	NCBI36
NG_031884.1:g.65134G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1861G>C MANE Select	ENSP00000382423.3:p.Gly621Arg
ENST00000399503.3:c.1861G>C	ENSP00000382423.3:p.Gly621Arg
NM_005921.1:c.1861G>C	NP_005912.1:p.Gly621Arg
XM_005248519.3:c.1483G>C	XP_005248576.2:p.Gly495Arg
XM_011543406.1:c.1606G>C	XP_011541708.1:p.Gly536Arg
XM_011543407.1:c.1686+2201G>C	XP_011541709.1:n.1686+2201G>C
XM_011543408.1:c.1861G>C	XP_011541710.1:p.Gly621Arg
XM_017009484.1:c.1450G>C	XP_016864973.1:p.Gly484Arg
XM_017009485.1:c.1372G>C	XP_016864974.1:p.Gly458Arg
XR_001742068.2:n.1892G>C
NM_005921.2:c.1861G>C MANE Select	NP_005912.1:p.Gly621Arg