Canonical Allele Identifier: CA500639176

Gene: MAP3K14 MAP3K14-AS1

Linked Data

• gnomAD v4: 17-45267434-C-G
• MyVariant Identifiers: chr17:g.43344801C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267434C>G , CM000679.2:g.45267434C>G	GRCh38
NC_000017.10:g.43344801C>G , CM000679.1:g.43344801C>G	GRCh37
NC_000017.9:g.40700584C>G	NCBI36
NG_033823.1:g.54615G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344686.8:c.2298G>C (MAP3K14) MANE Select	ENSP00000478552.1:p.Pro766=
ENST00000586644.2:n.1235G>C (MAP3K14)
ENST00000617331.3:c.2298G>C (MAP3K14)	ENSP00000480974.3:p.Pro766=
ENST00000680632.1:c.1352G>C (MAP3K14)	ENSP00000505027.1:n.1352G>C
ENST00000344686.6:c.2298G>C (MAP3K14)	ENSP00000478552.1:p.Pro766=
ENST00000376926.8:c.2298G>C (MAP3K14)	ENSP00000482657.1:p.Pro766=
ENST00000592267.1:n.1105G>C (MAP3K14)
NM_003954.4:c.2298G>C (MAP3K14)	NP_003945.2:p.Pro766=
NR_024434.2:n.295+106C>G (MAP3K14-AS1)
NR_024435.2:n.749+106C>G (MAP3K14-AS1)
NR_110324.1:n.480+106C>G (MAP3K14-AS1)
NR_110325.1:n.475+106C>G (MAP3K14-AS1)
NR_110326.1:n.379+106C>G (MAP3K14-AS1)
XM_011525441.1:c.2298G>C (MAP3K14)	XP_011523743.1:p.Pro766=
XR_934591.1:n.2613G>C (MAP3K14)
NM_003954.5:c.2298G>C (MAP3K14) MANE Select	NP_003945.2:p.Pro766=
XM_011525441.2:c.2298G>C (MAP3K14)	XP_011523743.1:p.Pro766=