Canonical Allele Identifier: CA399874762

Gene: MAP3K14 MAP3K14-AS1

Linked Data

• gnomAD v4: 17-45267430-G-T
• MyVariant Identifiers: chr17:g.43344797G>T (hg19) ; chr17:g.45267430G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267430G>T , CM000679.2:g.45267430G>T	GRCh38
NC_000017.10:g.43344797G>T , CM000679.1:g.43344797G>T	GRCh37
NC_000017.9:g.40700580G>T	NCBI36
NG_033823.1:g.54619C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344686.8:c.2302C>A (MAP3K14) MANE Select	ENSP00000478552.1:p.Gln768Lys
ENST00000586644.2:n.1239C>A (MAP3K14)
ENST00000617331.3:c.2302C>A (MAP3K14)	ENSP00000480974.3:p.Gln768Lys
ENST00000680632.1:c.1356C>A (MAP3K14)	ENSP00000505027.1:n.1356C>A
ENST00000344686.6:c.2302C>A (MAP3K14)	ENSP00000478552.1:p.Gln768Lys
ENST00000376926.8:c.2302C>A (MAP3K14)	ENSP00000482657.1:p.Gln768Lys
ENST00000592267.1:n.1109C>A (MAP3K14)
NM_003954.4:c.2302C>A (MAP3K14)	NP_003945.2:p.Gln768Lys
NR_024434.2:n.295+102G>T (MAP3K14-AS1)
NR_024435.2:n.749+102G>T (MAP3K14-AS1)
NR_110324.1:n.480+102G>T (MAP3K14-AS1)
NR_110325.1:n.475+102G>T (MAP3K14-AS1)
NR_110326.1:n.379+102G>T (MAP3K14-AS1)
XM_011525441.1:c.2302C>A (MAP3K14)	XP_011523743.1:p.Gln768Lys
XR_934591.1:n.2617C>A (MAP3K14)
NM_003954.5:c.2302C>A (MAP3K14) MANE Select	NP_003945.2:p.Gln768Lys
XM_011525441.2:c.2302C>A (MAP3K14)	XP_011523743.1:p.Gln768Lys