Canonical Allele Identifier: CA500639107

Gene: MAP3K14 MAP3K14-AS1

Linked Data

• MyVariant Identifiers: chr17:g.43344691C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267324C>A , CM000679.2:g.45267324C>A	GRCh38
NC_000017.10:g.43344691C>A , CM000679.1:g.43344691C>A	GRCh37
NC_000017.9:g.40700474C>A	NCBI36
NG_033823.1:g.54725G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344686.8:c.2326+82G>T (MAP3K14) MANE Select	ENSP00000478552.1:n.2326+82G>T
ENST00000586644.2:n.1263+82G>T (MAP3K14)
ENST00000617331.3:c.2326+82G>T (MAP3K14)	ENSP00000480974.3:n.2326+82G>T
ENST00000680632.1:c.1380+82G>T (MAP3K14)	ENSP00000505027.1:n.1380+82G>T
ENST00000344686.6:c.2326+82G>T (MAP3K14)	ENSP00000478552.1:n.2326+82G>T
ENST00000376926.8:c.2326+82G>T (MAP3K14)	ENSP00000482657.1:n.2326+82G>T
ENST00000592267.1:n.1133+82G>T (MAP3K14)
NM_003954.4:c.2326+82G>T (MAP3K14)	NP_003945.2:n.2326+82G>T
NR_024434.2:n.291C>A (MAP3K14-AS1)
NR_024435.2:n.745C>A (MAP3K14-AS1)
NR_110324.1:n.476C>A (MAP3K14-AS1)
NR_110325.1:n.471C>A (MAP3K14-AS1)
NR_110326.1:n.375C>A (MAP3K14-AS1)
XM_011525441.1:c.2326+82G>T (MAP3K14)	XP_011523743.1:n.2326+82G>T
XR_934591.1:n.2641+82G>T (MAP3K14)
NM_003954.5:c.2326+82G>T (MAP3K14) MANE Select	NP_003945.2:n.2326+82G>T
XM_011525441.2:c.2326+82G>T (MAP3K14)	XP_011523743.1:n.2326+82G>T