Canonical Allele Identifier: CA359787743

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111945992
• MyVariant Identifiers: chr5:g.56178166A>T (hg19) ; chr5:g.56882339A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882339A>T , CM000667.2:g.56882339A>T	GRCh38
NC_000005.9:g.56178166A>T , CM000667.1:g.56178166A>T	GRCh37
NC_000005.8:g.56213923A>T	NCBI36
NG_031884.1:g.72267A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3139A>T MANE Select	ENSP00000382423.3:p.Thr1047Ser
ENST00000399503.3:c.3139A>T	ENSP00000382423.3:p.Thr1047Ser
NM_005921.1:c.3139A>T	NP_005912.1:p.Thr1047Ser
XM_005248519.3:c.2761A>T	XP_005248576.2:p.Thr921Ser
XM_011543406.1:c.2884A>T	XP_011541708.1:p.Thr962Ser
XM_011543407.1:c.2860A>T	XP_011541709.1:p.Thr954Ser
XM_011543408.1:c.3139A>T	XP_011541710.1:p.Thr1047Ser
XM_017009484.1:c.2728A>T	XP_016864973.1:p.Thr910Ser
XM_017009485.1:c.2650A>T	XP_016864974.1:p.Thr884Ser
XR_001742068.2:n.3170A>T
NM_005921.2:c.3139A>T MANE Select	NP_005912.1:p.Thr1047Ser