Canonical Allele Identifier: CA359787884

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178232A>T (hg19) ; chr5:g.56882405A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882405A>T , CM000667.2:g.56882405A>T	GRCh38
NC_000005.9:g.56178232A>T , CM000667.1:g.56178232A>T	GRCh37
NC_000005.8:g.56213989A>T	NCBI36
NG_031884.1:g.72333A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3205A>T MANE Select	ENSP00000382423.3:p.Asn1069Tyr
ENST00000399503.3:c.3205A>T	ENSP00000382423.3:p.Asn1069Tyr
NM_005921.1:c.3205A>T	NP_005912.1:p.Asn1069Tyr
XM_005248519.3:c.2827A>T	XP_005248576.2:p.Asn943Tyr
XM_011543406.1:c.2950A>T	XP_011541708.1:p.Asn984Tyr
XM_011543407.1:c.2926A>T	XP_011541709.1:p.Asn976Tyr
XM_011543408.1:c.3205A>T	XP_011541710.1:p.Asn1069Tyr
XM_017009484.1:c.2794A>T	XP_016864973.1:p.Asn932Tyr
XM_017009485.1:c.2716A>T	XP_016864974.1:p.Asn906Tyr
XR_001742068.2:n.3236A>T
NM_005921.2:c.3205A>T MANE Select	NP_005912.1:p.Asn1069Tyr