Canonical Allele Identifier: CA500639120

Gene: MAP3K14 MAP3K14-AS1

Linked Data

• MyVariant Identifiers: chr17:g.43344694A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267327A>G , CM000679.2:g.45267327A>G	GRCh38
NC_000017.10:g.43344694A>G , CM000679.1:g.43344694A>G	GRCh37
NC_000017.9:g.40700477A>G	NCBI36
NG_033823.1:g.54722T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.2326+79T>C (MAP3K14) MANE Select	ENSP00000478552.1:n.2326+79T>C
ENST00000586644.2:n.1263+79T>C (MAP3K14)
ENST00000617331.3:c.2326+79T>C (MAP3K14)	ENSP00000480974.3:n.2326+79T>C
ENST00000680632.1:c.1380+79T>C (MAP3K14)	ENSP00000505027.1:n.1380+79T>C
ENST00000344686.6:c.2326+79T>C (MAP3K14)	ENSP00000478552.1:n.2326+79T>C
ENST00000376926.8:c.2326+79T>C (MAP3K14)	ENSP00000482657.1:n.2326+79T>C
ENST00000592267.1:n.1133+79T>C (MAP3K14)
NM_003954.4:c.2326+79T>C (MAP3K14)	NP_003945.2:n.2326+79T>C
NR_024434.2:n.294A>G (MAP3K14-AS1)
NR_024435.2:n.748A>G (MAP3K14-AS1)
NR_110324.1:n.479A>G (MAP3K14-AS1)
NR_110325.1:n.474A>G (MAP3K14-AS1)
NR_110326.1:n.378A>G (MAP3K14-AS1)
XM_011525441.1:c.2326+79T>C (MAP3K14)	XP_011523743.1:n.2326+79T>C
XR_934591.1:n.2641+79T>C (MAP3K14)
NM_003954.5:c.2326+79T>C (MAP3K14) MANE Select	NP_003945.2:n.2326+79T>C
XM_011525441.2:c.2326+79T>C (MAP3K14)	XP_011523743.1:n.2326+79T>C