Canonical Allele Identifier: CA444391489

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155503A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859676A>T , CM000667.2:g.56859676A>T	GRCh38
NC_000005.9:g.56155503A>T , CM000667.1:g.56155503A>T	GRCh37
NC_000005.8:g.56191260A>T	NCBI36
NG_031884.1:g.49604A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.634-39A>T MANE Select	ENSP00000382423.3:n.634-39A>T
ENST00000399503.3:c.634-39A>T	ENSP00000382423.3:n.634-39A>T
NM_005921.1:c.634-39A>T	NP_005912.1:n.634-39A>T
XM_005248519.3:c.256-39A>T	XP_005248576.2:n.256-39A>T
XM_011543406.1:c.379-39A>T	XP_011541708.1:n.379-39A>T
XM_011543407.1:c.634-39A>T	XP_011541709.1:n.634-39A>T
XM_011543408.1:c.634-39A>T	XP_011541710.1:n.634-39A>T
XM_017009484.1:c.223-39A>T	XP_016864973.1:n.223-39A>T
XM_017009485.1:c.145-39A>T	XP_016864974.1:n.145-39A>T
XR_001742068.2:n.665-39A>T
NM_005921.2:c.634-39A>T MANE Select	NP_005912.1:n.634-39A>T