Canonical Allele Identifier: CA291084378

Gene: MAP3K14

Linked Data

• dbSNP Id: rs9906772
• gnomAD v2: 17-43383524-G-A
• gnomAD v3: 17-45306158-G-A
• gnomAD v4: 17-45306158-G-A
• MyVariant Identifiers: chr17:g.43383524G>A (hg19) ; chr17:g.45306158G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45306158G>A , CM000679.2:g.45306158G>A	GRCh38
NC_000017.10:g.43383524G>A , CM000679.1:g.43383524G>A	GRCh37
NC_000017.9:g.40739307G>A	NCBI36
NG_033823.1:g.15891C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000344686.8:c.-21+10802C>T MANE Select	ENSP00000478552.1:n.-21+10802C>T
ENST00000617331.3:c.-21+6127C>T	ENSP00000480974.3:n.-21+6127C>T
ENST00000344686.6:c.-21+10802C>T	ENSP00000478552.1:n.-21+10802C>T
ENST00000617331.1:c.-21+10802C>T	ENSP00000480974.1:n.-21+10802C>T
NM_003954.4:c.-21+10802C>T	NP_003945.2:n.-21+10802C>T
XM_011525441.1:c.-21+6127C>T	XP_011523743.1:n.-21+6127C>T
XR_934591.1:n.89+10802C>T
NM_003954.5:c.-21+10802C>T MANE Select	NP_003945.2:n.-21+10802C>T
XM_011525441.2:c.-21+6127C>T	XP_011523743.1:n.-21+6127C>T