Canonical Allele Identifier: CA444398889

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171101T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875274T>C , CM000667.2:g.56875274T>C	GRCh38
NC_000005.9:g.56171101T>C , CM000667.1:g.56171101T>C	GRCh37
NC_000005.8:g.56206858T>C	NCBI36
NG_031884.1:g.65202T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1929T>C MANE Select	ENSP00000382423.3:p.Cys643=
ENST00000399503.3:c.1929T>C	ENSP00000382423.3:p.Cys643=
NM_005921.1:c.1929T>C	NP_005912.1:p.Cys643=
XM_005248519.3:c.1551T>C	XP_005248576.2:p.Cys517=
XM_011543406.1:c.1674T>C	XP_011541708.1:p.Cys558=
XM_011543407.1:c.1686+2269T>C	XP_011541709.1:n.1686+2269T>C
XM_011543408.1:c.1929T>C	XP_011541710.1:p.Cys643=
XM_017009484.1:c.1518T>C	XP_016864973.1:p.Cys506=
XM_017009485.1:c.1440T>C	XP_016864974.1:p.Cys480=
XR_001742068.2:n.1960T>C
NM_005921.2:c.1929T>C MANE Select	NP_005912.1:p.Cys643=