Canonical Allele Identifier: CA291055847

Gene: MAP3K14 MAP3K14-AS1

Linked Data

• ClinVar Variation Id: 544324
• ClinVar RCV Id: RCV000655444
• dbSNP Id: rs148416800
• MyVariant Identifiers: chr17:g.43344787T>G (hg19) ; chr17:g.45267420T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267420T>G , CM000679.2:g.45267420T>G	GRCh38
NC_000017.10:g.43344787T>G , CM000679.1:g.43344787T>G	GRCh37
NC_000017.9:g.40700570T>G	NCBI36
NG_033823.1:g.54629A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344686.8:c.2312A>C (MAP3K14) MANE Select	ENSP00000478552.1:p.Gln771Pro
ENST00000586644.2:n.1249A>C (MAP3K14)
ENST00000617331.3:c.2312A>C (MAP3K14)	ENSP00000480974.3:p.Gln771Pro
ENST00000680632.1:c.1366A>C (MAP3K14)	ENSP00000505027.1:n.1366A>C
ENST00000344686.6:c.2312A>C (MAP3K14)	ENSP00000478552.1:p.Gln771Pro
ENST00000376926.8:c.2312A>C (MAP3K14)	ENSP00000482657.1:p.Gln771Pro
ENST00000592267.1:n.1119A>C (MAP3K14)
NM_003954.4:c.2312A>C (MAP3K14)	NP_003945.2:p.Gln771Pro
NR_024434.2:n.295+92T>G (MAP3K14-AS1)
NR_024435.2:n.749+92T>G (MAP3K14-AS1)
NR_110324.1:n.480+92T>G (MAP3K14-AS1)
NR_110325.1:n.475+92T>G (MAP3K14-AS1)
NR_110326.1:n.379+92T>G (MAP3K14-AS1)
XM_011525441.1:c.2312A>C (MAP3K14)	XP_011523743.1:p.Gln771Pro
XR_934591.1:n.2627A>C (MAP3K14)
NM_003954.5:c.2312A>C (MAP3K14) MANE Select	NP_003945.2:p.Gln771Pro
XM_011525441.2:c.2312A>C (MAP3K14)	XP_011523743.1:p.Gln771Pro