Canonical Allele Identifier: CA2126961027
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30889830G= , CM000676.2:g.30889830G= GRCh38
NC_000014.8:g.31359036G= , CM000676.1:g.31359036G= GRCh37
NC_000014.7:g.30428787G= NCBI36
NG_008211.2:g.20296G=

Transcript Alleles

HGVS Amino-acid change
ENST00000216361.9:c.*39G= ENSP00000216361.5:n.*39G=
ENST00000396618.9:c.*39G= MANE Select ENSP00000379862.3:n.*39G=
ENST00000555117.2:c.1534+3518G= ENSP00000493569.1:n.1534+3518G=
ENST00000643575.1:c.*2+37G= ENSP00000494838.1:n.*2+37G=
ENST00000643697.1:n.1994G=
ENST00000644874.2:c.*39G= ENSP00000496360.1:n.*39G=
ENST00000216361.8:c.*39G= ENSP00000216361.4:n.*39G=
ENST00000396618.7:c.*39G= ENSP00000379862.3:n.*39G=
ENST00000460581.6:c.*39G= ENSP00000451713.1:n.*39G=
ENST00000468826.2:c.1343G=
ENST00000475087.5:c.1477+3518G= ENSP00000451528.1:n.1477+3518G=
NM_001135058.1:c.*39G= NP_001128530.1:n.*39G=
NM_004086.2:c.*39G= NP_004077.1:n.*39G=
XM_011536539.1:c.*2+37G= XP_011534841.1:n.*2+37G=
NM_001347720.1:c.*39G= NP_001334649.1:n.*39G=
XM_017021071.1:c.*39G= XP_016876560.1:n.*39G=
XM_024449506.1:c.*39G= XP_024305274.1:n.*39G=
NM_004086.3:c.*39G= MANE Select NP_004077.1:n.*39G=
NM_001135058.2:c.*39G= NP_001128530.1:n.*39G=
NM_001347720.2:c.*39G= NP_001334649.1:n.*39G=