Canonical Allele Identifier: CA2261795582

Gene: MAP3K14

Linked Data

• dbSNP Id: rs2044427737

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45306042T>C , CM000679.2:g.45306042T>C	GRCh38
NC_000017.10:g.43383408T>C , CM000679.1:g.43383408T>C	GRCh37
NC_000017.9:g.40739191T>C	NCBI36
NG_033823.1:g.16007A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.-21+10918A>G MANE Select	ENSP00000478552.1:n.-21+10918A>G
ENST00000617331.3:c.-21+6243A>G	ENSP00000480974.3:n.-21+6243A>G
ENST00000344686.6:c.-21+10918A>G	ENSP00000478552.1:n.-21+10918A>G
ENST00000617331.1:c.-21+10918A>G	ENSP00000480974.1:n.-21+10918A>G
NM_003954.4:c.-21+10918A>G	NP_003945.2:n.-21+10918A>G
XM_011525441.1:c.-21+6243A>G	XP_011523743.1:n.-21+6243A>G
XR_934591.1:n.89+10918A>G
NM_003954.5:c.-21+10918A>G MANE Select	NP_003945.2:n.-21+10918A>G
XM_011525441.2:c.-21+6243A>G	XP_011523743.1:n.-21+6243A>G