Canonical Allele Identifier: CA359787771

Gene: MAP3K1

Linked Data

• dbSNP Id: rs2111946077
• MyVariant Identifiers: chr5:g.56178179C>T (hg19) ; chr5:g.56882352C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882352C>T , CM000667.2:g.56882352C>T	GRCh38
NC_000005.9:g.56178179C>T , CM000667.1:g.56178179C>T	GRCh37
NC_000005.8:g.56213936C>T	NCBI36
NG_031884.1:g.72280C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3152C>T MANE Select	ENSP00000382423.3:p.Pro1051Leu
ENST00000399503.3:c.3152C>T	ENSP00000382423.3:p.Pro1051Leu
NM_005921.1:c.3152C>T	NP_005912.1:p.Pro1051Leu
XM_005248519.3:c.2774C>T	XP_005248576.2:p.Pro925Leu
XM_011543406.1:c.2897C>T	XP_011541708.1:p.Pro966Leu
XM_011543407.1:c.2873C>T	XP_011541709.1:p.Pro958Leu
XM_011543408.1:c.3152C>T	XP_011541710.1:p.Pro1051Leu
XM_017009484.1:c.2741C>T	XP_016864973.1:p.Pro914Leu
XM_017009485.1:c.2663C>T	XP_016864974.1:p.Pro888Leu
XR_001742068.2:n.3183C>T
NM_005921.2:c.3152C>T MANE Select	NP_005912.1:p.Pro1051Leu