Canonical Allele Identifier: CA359781075

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171034G>T (hg19) ; chr5:g.56875207G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875207G>T , CM000667.2:g.56875207G>T	GRCh38
NC_000005.9:g.56171034G>T , CM000667.1:g.56171034G>T	GRCh37
NC_000005.8:g.56206791G>T	NCBI36
NG_031884.1:g.65135G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1862G>T MANE Select	ENSP00000382423.3:p.Gly621Val
ENST00000399503.3:c.1862G>T	ENSP00000382423.3:p.Gly621Val
NM_005921.1:c.1862G>T	NP_005912.1:p.Gly621Val
XM_005248519.3:c.1484G>T	XP_005248576.2:p.Gly495Val
XM_011543406.1:c.1607G>T	XP_011541708.1:p.Gly536Val
XM_011543407.1:c.1686+2202G>T	XP_011541709.1:n.1686+2202G>T
XM_011543408.1:c.1862G>T	XP_011541710.1:p.Gly621Val
XM_017009484.1:c.1451G>T	XP_016864973.1:p.Gly484Val
XM_017009485.1:c.1373G>T	XP_016864974.1:p.Gly458Val
XR_001742068.2:n.1893G>T
NM_005921.2:c.1862G>T MANE Select	NP_005912.1:p.Gly621Val