Canonical Allele Identifier: CA399874752

Gene: MAP3K14 MAP3K14-AS1

Linked Data

• MyVariant Identifiers: chr17:g.43344796T>A (hg19) ; chr17:g.45267429T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267429T>A , CM000679.2:g.45267429T>A	GRCh38
NC_000017.10:g.43344796T>A , CM000679.1:g.43344796T>A	GRCh37
NC_000017.9:g.40700579T>A	NCBI36
NG_033823.1:g.54620A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.2303A>T (MAP3K14) MANE Select	ENSP00000478552.1:p.Gln768Leu
ENST00000586644.2:n.1240A>T (MAP3K14)
ENST00000617331.3:c.2303A>T (MAP3K14)	ENSP00000480974.3:p.Gln768Leu
ENST00000680632.1:c.1357A>T (MAP3K14)	ENSP00000505027.1:n.1357A>T
ENST00000344686.6:c.2303A>T (MAP3K14)	ENSP00000478552.1:p.Gln768Leu
ENST00000376926.8:c.2303A>T (MAP3K14)	ENSP00000482657.1:p.Gln768Leu
ENST00000592267.1:n.1110A>T (MAP3K14)
NM_003954.4:c.2303A>T (MAP3K14)	NP_003945.2:p.Gln768Leu
NR_024434.2:n.295+101T>A (MAP3K14-AS1)
NR_024435.2:n.749+101T>A (MAP3K14-AS1)
NR_110324.1:n.480+101T>A (MAP3K14-AS1)
NR_110325.1:n.475+101T>A (MAP3K14-AS1)
NR_110326.1:n.379+101T>A (MAP3K14-AS1)
XM_011525441.1:c.2303A>T (MAP3K14)	XP_011523743.1:p.Gln768Leu
XR_934591.1:n.2618A>T (MAP3K14)
NM_003954.5:c.2303A>T (MAP3K14) MANE Select	NP_003945.2:p.Gln768Leu
XM_011525441.2:c.2303A>T (MAP3K14)	XP_011523743.1:p.Gln768Leu