Canonical Allele Identifier: CA2126960923
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30889772T= , CM000676.2:g.30889772T= GRCh38
NC_000014.8:g.31358978T= , CM000676.1:g.31358978T= GRCh37
NC_000014.7:g.30428729T= NCBI36
NG_008211.2:g.20238T=

Transcript Alleles

HGVS Amino-acid change
ENST00000216361.9:c.1829T= ENSP00000216361.5:p.Phe610=
ENST00000396618.9:c.1634T= MANE Select ENSP00000379862.3:p.Phe545=
ENST00000555117.2:c.1534+3460T= ENSP00000493569.1:n.1534+3460T=
ENST00000643575.1:c.1634T= ENSP00000494838.1:p.Phe545=
ENST00000643697.1:n.1936T=
ENST00000644874.2:c.1634T= ENSP00000496360.1:p.Phe545=
ENST00000216361.8:c.1634T= ENSP00000216361.4:p.Phe545=
ENST00000396618.7:c.1634T= ENSP00000379862.3:p.Phe545=
ENST00000460581.6:c.1298T= ENSP00000451713.1:p.Phe433=
ENST00000468826.2:c.1285T=
ENST00000475087.5:c.1477+3460T= ENSP00000451528.1:n.1477+3460T=
NM_001135058.1:c.1634T= NP_001128530.1:p.Phe545=
NM_004086.2:c.1634T= NP_004077.1:p.Phe545=
NR_038356.1:n.37A=
XM_011536539.1:c.1634T= XP_011534841.1:p.Phe545=
NM_001347720.1:c.1829T= NP_001334649.1:p.Phe610=
XM_017021071.1:c.1829T= XP_016876560.1:p.Phe610=
XM_024449506.1:c.1691T= XP_024305274.1:p.Phe564=
NM_004086.3:c.1634T= MANE Select NP_004077.1:p.Phe545=
NM_001135058.2:c.1634T= NP_001128530.1:p.Phe545=
NM_001347720.2:c.1829T= NP_001334649.1:p.Phe610=