Canonical Allele Identifier: CA772381178

Gene: MAP3K14

Linked Data

• dbSNP Id: rs1353834423
• gnomAD v3: 17-45306049-T-G
• gnomAD v4: 17-45306049-T-G
• MyVariant Identifiers: chr17:g.43383415T>G (hg19) ; chr17:g.45306049T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45306049T>G , CM000679.2:g.45306049T>G	GRCh38
NC_000017.10:g.43383415T>G , CM000679.1:g.43383415T>G	GRCh37
NC_000017.9:g.40739198T>G	NCBI36
NG_033823.1:g.16000A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344686.8:c.-21+10911A>C MANE Select	ENSP00000478552.1:n.-21+10911A>C
ENST00000617331.3:c.-21+6236A>C	ENSP00000480974.3:n.-21+6236A>C
ENST00000344686.6:c.-21+10911A>C	ENSP00000478552.1:n.-21+10911A>C
ENST00000617331.1:c.-21+10911A>C	ENSP00000480974.1:n.-21+10911A>C
NM_003954.4:c.-21+10911A>C	NP_003945.2:n.-21+10911A>C
XM_011525441.1:c.-21+6236A>C	XP_011523743.1:n.-21+6236A>C
XR_934591.1:n.89+10911A>C
NM_003954.5:c.-21+10911A>C MANE Select	NP_003945.2:n.-21+10911A>C
XM_011525441.2:c.-21+6236A>C	XP_011523743.1:n.-21+6236A>C