Canonical Allele Identifier: CA359802326

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155549A>T (hg19) ; chr5:g.56859722A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859722A>T , CM000667.2:g.56859722A>T	GRCh38
NC_000005.9:g.56155549A>T , CM000667.1:g.56155549A>T	GRCh37
NC_000005.8:g.56191306A>T	NCBI36
NG_031884.1:g.49650A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.641A>T MANE Select	ENSP00000382423.3:p.Lys214Ile
ENST00000399503.3:c.641A>T	ENSP00000382423.3:p.Lys214Ile
NM_005921.1:c.641A>T	NP_005912.1:p.Lys214Ile
XM_005248519.3:c.263A>T	XP_005248576.2:p.Lys88Ile
XM_011543406.1:c.386A>T	XP_011541708.1:p.Lys129Ile
XM_011543407.1:c.641A>T	XP_011541709.1:p.Lys214Ile
XM_011543408.1:c.641A>T	XP_011541710.1:p.Lys214Ile
XM_017009484.1:c.230A>T	XP_016864973.1:p.Lys77Ile
XM_017009485.1:c.152A>T	XP_016864974.1:p.Lys51Ile
XR_001742068.2:n.672A>T
NM_005921.2:c.641A>T MANE Select	NP_005912.1:p.Lys214Ile