Canonical Allele Identifier: CA359787856

Gene: MAP3K1

Linked Data

• gnomAD v4: 5-56882391-G-C
• MyVariant Identifiers: chr5:g.56178218G>C (hg19) ; chr5:g.56882391G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882391G>C , CM000667.2:g.56882391G>C	GRCh38
NC_000005.9:g.56178218G>C , CM000667.1:g.56178218G>C	GRCh37
NC_000005.8:g.56213975G>C	NCBI36
NG_031884.1:g.72319G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3191G>C MANE Select	ENSP00000382423.3:p.Arg1064Thr
ENST00000399503.3:c.3191G>C	ENSP00000382423.3:p.Arg1064Thr
NM_005921.1:c.3191G>C	NP_005912.1:p.Arg1064Thr
XM_005248519.3:c.2813G>C	XP_005248576.2:p.Arg938Thr
XM_011543406.1:c.2936G>C	XP_011541708.1:p.Arg979Thr
XM_011543407.1:c.2912G>C	XP_011541709.1:p.Arg971Thr
XM_011543408.1:c.3191G>C	XP_011541710.1:p.Arg1064Thr
XM_017009484.1:c.2780G>C	XP_016864973.1:p.Arg927Thr
XM_017009485.1:c.2702G>C	XP_016864974.1:p.Arg901Thr
XR_001742068.2:n.3222G>C
NM_005921.2:c.3191G>C MANE Select	NP_005912.1:p.Arg1064Thr