Canonical Allele Identifier: CA772381184

Gene: MAP3K14

Linked Data

• dbSNP Id: rs1245738718
• MyVariant Identifiers: chr17:g.43383443A>G (hg19) ; chr17:g.45306077A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45306077A>G , CM000679.2:g.45306077A>G	GRCh38
NC_000017.10:g.43383443A>G , CM000679.1:g.43383443A>G	GRCh37
NC_000017.9:g.40739226A>G	NCBI36
NG_033823.1:g.15972T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.-21+10883T>C MANE Select	ENSP00000478552.1:n.-21+10883T>C
ENST00000617331.3:c.-21+6208T>C	ENSP00000480974.3:n.-21+6208T>C
ENST00000344686.6:c.-21+10883T>C	ENSP00000478552.1:n.-21+10883T>C
ENST00000617331.1:c.-21+10883T>C	ENSP00000480974.1:n.-21+10883T>C
NM_003954.4:c.-21+10883T>C	NP_003945.2:n.-21+10883T>C
XM_011525441.1:c.-21+6208T>C	XP_011523743.1:n.-21+6208T>C
XR_934591.1:n.89+10883T>C
NM_003954.5:c.-21+10883T>C MANE Select	NP_003945.2:n.-21+10883T>C
XM_011525441.2:c.-21+6208T>C	XP_011523743.1:n.-21+6208T>C