Canonical Allele Identifier: CA444399798

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178147T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882320T>C , CM000667.2:g.56882320T>C	GRCh38
NC_000005.9:g.56178147T>C , CM000667.1:g.56178147T>C	GRCh37
NC_000005.8:g.56213904T>C	NCBI36
NG_031884.1:g.72248T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3120T>C MANE Select	ENSP00000382423.3:p.Asp1040=
ENST00000399503.3:c.3120T>C	ENSP00000382423.3:p.Asp1040=
NM_005921.1:c.3120T>C	NP_005912.1:p.Asp1040=
XM_005248519.3:c.2742T>C	XP_005248576.2:p.Asp914=
XM_011543406.1:c.2865T>C	XP_011541708.1:p.Asp955=
XM_011543407.1:c.2841T>C	XP_011541709.1:p.Asp947=
XM_011543408.1:c.3120T>C	XP_011541710.1:p.Asp1040=
XM_017009484.1:c.2709T>C	XP_016864973.1:p.Asp903=
XM_017009485.1:c.2631T>C	XP_016864974.1:p.Asp877=
XR_001742068.2:n.3151T>C
NM_005921.2:c.3120T>C MANE Select	NP_005912.1:p.Asp1040=