Canonical Allele Identifier: CA1057381843

Linked Data

dbSNP Id: rs1714584438

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186106237T>C , CM000665.2:g.186106237T>C GRCh38
NC_000003.11:g.185824026T>C , CM000665.1:g.185824026T>C GRCh37
NC_000003.10:g.187306720T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306376.10:c.-74-295A>G (ETV5) MANE Select ENSP00000306894.5:n.-74-295A>G
ENST00000306376.9:c.-74-295A>G (ETV5) ENSP00000306894.5:n.-74-295A>G
ENST00000413301.5:c.-74-295A>G (ETV5) ENSP00000405157.1:n.-74-295A>G
ENST00000421809.5:c.-74-295A>G (ETV5) ENSP00000412171.1:n.-74-295A>G
ENST00000422039.1:c.-74-295A>G (ETV5) ENSP00000388737.1:n.-74-295A>G
ENST00000434744.5:c.-74-295A>G (ETV5) ENSP00000413755.1:n.-74-295A>G
ENST00000440773.5:c.-74-295A>G (ETV5) ENSP00000389707.1:n.-74-295A>G
ENST00000447054.5:n.132-295A>G (DGKG)
ENST00000476890.1:n.143-295A>G (ETV5)
NM_004454.2:c.-74-295A>G (ETV5) NP_004445.1:n.-74-295A>G
NM_004454.3:c.-74-295A>G (ETV5) MANE Select NP_004445.1:n.-74-295A>G