Canonical Allele Identifier: CA444398779

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56875199-C-T
• MyVariant Identifiers: chr5:g.56171026C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875199C>T , CM000667.2:g.56875199C>T	GRCh38
NC_000005.9:g.56171026C>T , CM000667.1:g.56171026C>T	GRCh37
NC_000005.8:g.56206783C>T	NCBI36
NG_031884.1:g.65127C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.1854C>T MANE Select	ENSP00000382423.3:p.Ala618=
ENST00000399503.3:c.1854C>T	ENSP00000382423.3:p.Ala618=
NM_005921.1:c.1854C>T	NP_005912.1:p.Ala618=
XM_005248519.3:c.1476C>T	XP_005248576.2:p.Ala492=
XM_011543406.1:c.1599C>T	XP_011541708.1:p.Ala533=
XM_011543407.1:c.1686+2194C>T	XP_011541709.1:n.1686+2194C>T
XM_011543408.1:c.1854C>T	XP_011541710.1:p.Ala618=
XM_017009484.1:c.1443C>T	XP_016864973.1:p.Ala481=
XM_017009485.1:c.1365C>T	XP_016864974.1:p.Ala455=
XR_001742068.2:n.1885C>T
NM_005921.2:c.1854C>T MANE Select	NP_005912.1:p.Ala618=