Canonical Allele Identifier: CA399874722

Gene: MAP3K14 MAP3K14-AS1

Linked Data

• gnomAD v4: 17-45267424-G-T
• MyVariant Identifiers: chr17:g.43344791G>T (hg19) ; chr17:g.45267424G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267424G>T , CM000679.2:g.45267424G>T	GRCh38
NC_000017.10:g.43344791G>T , CM000679.1:g.43344791G>T	GRCh37
NC_000017.9:g.40700574G>T	NCBI36
NG_033823.1:g.54625C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.2308C>A (MAP3K14) MANE Select	ENSP00000478552.1:p.Leu770Met
ENST00000586644.2:n.1245C>A (MAP3K14)
ENST00000617331.3:c.2308C>A (MAP3K14)	ENSP00000480974.3:p.Leu770Met
ENST00000680632.1:c.1362C>A (MAP3K14)	ENSP00000505027.1:n.1362C>A
ENST00000344686.6:c.2308C>A (MAP3K14)	ENSP00000478552.1:p.Leu770Met
ENST00000376926.8:c.2308C>A (MAP3K14)	ENSP00000482657.1:p.Leu770Met
ENST00000592267.1:n.1115C>A (MAP3K14)
NM_003954.4:c.2308C>A (MAP3K14)	NP_003945.2:p.Leu770Met
NR_024434.2:n.295+96G>T (MAP3K14-AS1)
NR_024435.2:n.749+96G>T (MAP3K14-AS1)
NR_110324.1:n.480+96G>T (MAP3K14-AS1)
NR_110325.1:n.475+96G>T (MAP3K14-AS1)
NR_110326.1:n.379+96G>T (MAP3K14-AS1)
XM_011525441.1:c.2308C>A (MAP3K14)	XP_011523743.1:p.Leu770Met
XR_934591.1:n.2623C>A (MAP3K14)
NM_003954.5:c.2308C>A (MAP3K14) MANE Select	NP_003945.2:p.Leu770Met
XM_011525441.2:c.2308C>A (MAP3K14)	XP_011523743.1:p.Leu770Met