Canonical Allele Identifier: CA444399222

Gene: MAP3K1

Linked Data

• dbSNP Id: rs1748217955
• MyVariant Identifiers: chr5:g.56177638T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881811T>C , CM000667.2:g.56881811T>C	GRCh38
NC_000005.9:g.56177638T>C , CM000667.1:g.56177638T>C	GRCh37
NC_000005.8:g.56213395T>C	NCBI36
NG_031884.1:g.71739T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2611T>C MANE Select	ENSP00000382423.3:p.Leu871=
ENST00000399503.3:c.2611T>C	ENSP00000382423.3:p.Leu871=
NM_005921.1:c.2611T>C	NP_005912.1:p.Leu871=
XM_005248519.3:c.2233T>C	XP_005248576.2:p.Leu745=
XM_011543406.1:c.2356T>C	XP_011541708.1:p.Leu786=
XM_011543407.1:c.2332T>C	XP_011541709.1:p.Leu778=
XM_011543408.1:c.2611T>C	XP_011541710.1:p.Leu871=
XM_017009484.1:c.2200T>C	XP_016864973.1:p.Leu734=
XM_017009485.1:c.2122T>C	XP_016864974.1:p.Leu708=
XR_001742068.2:n.2642T>C
NM_005921.2:c.2611T>C MANE Select	NP_005912.1:p.Leu871=