Canonical Allele Identifier: CA359786135

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177623G>T (hg19) ; chr5:g.56881796G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881796G>T , CM000667.2:g.56881796G>T	GRCh38
NC_000005.9:g.56177623G>T , CM000667.1:g.56177623G>T	GRCh37
NC_000005.8:g.56213380G>T	NCBI36
NG_031884.1:g.71724G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2596G>T MANE Select	ENSP00000382423.3:p.Ala866Ser
ENST00000399503.3:c.2596G>T	ENSP00000382423.3:p.Ala866Ser
NM_005921.1:c.2596G>T	NP_005912.1:p.Ala866Ser
XM_005248519.3:c.2218G>T	XP_005248576.2:p.Ala740Ser
XM_011543406.1:c.2341G>T	XP_011541708.1:p.Ala781Ser
XM_011543407.1:c.2317G>T	XP_011541709.1:p.Ala773Ser
XM_011543408.1:c.2596G>T	XP_011541710.1:p.Ala866Ser
XM_017009484.1:c.2185G>T	XP_016864973.1:p.Ala729Ser
XM_017009485.1:c.2107G>T	XP_016864974.1:p.Ala703Ser
XR_001742068.2:n.2627G>T
NM_005921.2:c.2596G>T MANE Select	NP_005912.1:p.Ala866Ser