Canonical Allele Identifier: CA291084297

Gene: MAP3K14

Linked Data

• dbSNP Id: rs540695912
• gnomAD v3: 17-45306093-T-C
• gnomAD v4: 17-45306093-T-C
• MyVariant Identifiers: chr17:g.43383459T>C (hg19) ; chr17:g.45306093T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45306093T>C , CM000679.2:g.45306093T>C	GRCh38
NC_000017.10:g.43383459T>C , CM000679.1:g.43383459T>C	GRCh37
NC_000017.9:g.40739242T>C	NCBI36
NG_033823.1:g.15956A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.-21+10867A>G MANE Select	ENSP00000478552.1:n.-21+10867A>G
ENST00000617331.3:c.-21+6192A>G	ENSP00000480974.3:n.-21+6192A>G
ENST00000344686.6:c.-21+10867A>G	ENSP00000478552.1:n.-21+10867A>G
ENST00000617331.1:c.-21+10867A>G	ENSP00000480974.1:n.-21+10867A>G
NM_003954.4:c.-21+10867A>G	NP_003945.2:n.-21+10867A>G
XM_011525441.1:c.-21+6192A>G	XP_011523743.1:n.-21+6192A>G
XR_934591.1:n.89+10867A>G
NM_003954.5:c.-21+10867A>G MANE Select	NP_003945.2:n.-21+10867A>G
XM_011525441.2:c.-21+6192A>G	XP_011523743.1:n.-21+6192A>G