Canonical Allele Identifier: CA359787745

Gene: MAP3K1

Linked Data

• dbSNP Id: rs755413206
• MyVariant Identifiers: chr5:g.56178167C>G (hg19) ; chr5:g.56882340C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882340C>G , CM000667.2:g.56882340C>G	GRCh38
NC_000005.9:g.56178167C>G , CM000667.1:g.56178167C>G	GRCh37
NC_000005.8:g.56213924C>G	NCBI36
NG_031884.1:g.72268C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3140C>G MANE Select	ENSP00000382423.3:p.Thr1047Ser
ENST00000399503.3:c.3140C>G	ENSP00000382423.3:p.Thr1047Ser
NM_005921.1:c.3140C>G	NP_005912.1:p.Thr1047Ser
XM_005248519.3:c.2762C>G	XP_005248576.2:p.Thr921Ser
XM_011543406.1:c.2885C>G	XP_011541708.1:p.Thr962Ser
XM_011543407.1:c.2861C>G	XP_011541709.1:p.Thr954Ser
XM_011543408.1:c.3140C>G	XP_011541710.1:p.Thr1047Ser
XM_017009484.1:c.2729C>G	XP_016864973.1:p.Thr910Ser
XM_017009485.1:c.2651C>G	XP_016864974.1:p.Thr884Ser
XR_001742068.2:n.3171C>G
NM_005921.2:c.3140C>G MANE Select	NP_005912.1:p.Thr1047Ser