Canonical Allele Identifier: CA291055801

Gene: MAP3K14 MAP3K14-AS1

Linked Data

• dbSNP Id: rs993551905
• gnomAD v3: 17-45267331-A-G
• gnomAD v4: 17-45267331-A-G
• MyVariant Identifiers: chr17:g.43344698A>G (hg19) ; chr17:g.45267331A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267331A>G , CM000679.2:g.45267331A>G	GRCh38
NC_000017.10:g.43344698A>G , CM000679.1:g.43344698A>G	GRCh37
NC_000017.9:g.40700481A>G	NCBI36
NG_033823.1:g.54718T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.2326+75T>C (MAP3K14) MANE Select	ENSP00000478552.1:n.2326+75T>C
ENST00000586644.2:n.1263+75T>C (MAP3K14)
ENST00000617331.3:c.2326+75T>C (MAP3K14)	ENSP00000480974.3:n.2326+75T>C
ENST00000680632.1:c.1380+75T>C (MAP3K14)	ENSP00000505027.1:n.1380+75T>C
ENST00000344686.6:c.2326+75T>C (MAP3K14)	ENSP00000478552.1:n.2326+75T>C
ENST00000376926.8:c.2326+75T>C (MAP3K14)	ENSP00000482657.1:n.2326+75T>C
ENST00000592267.1:n.1133+75T>C (MAP3K14)
NM_003954.4:c.2326+75T>C (MAP3K14)	NP_003945.2:n.2326+75T>C
NR_024434.2:n.295+3A>G (MAP3K14-AS1)
NR_024435.2:n.749+3A>G (MAP3K14-AS1)
NR_110324.1:n.480+3A>G (MAP3K14-AS1)
NR_110325.1:n.475+3A>G (MAP3K14-AS1)
NR_110326.1:n.379+3A>G (MAP3K14-AS1)
XM_011525441.1:c.2326+75T>C (MAP3K14)	XP_011523743.1:n.2326+75T>C
XR_934591.1:n.2641+75T>C (MAP3K14)
NM_003954.5:c.2326+75T>C (MAP3K14) MANE Select	NP_003945.2:n.2326+75T>C
XM_011525441.2:c.2326+75T>C (MAP3K14)	XP_011523743.1:n.2326+75T>C