Canonical Allele Identifier: CA389349572
Gene: COCH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30889683A>C , CM000676.2:g.30889683A>C GRCh38
NC_000014.8:g.31358889A>C , CM000676.1:g.31358889A>C GRCh37
NC_000014.7:g.30428640A>C NCBI36
NG_008211.2:g.20149A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216361.9:c.1740A>C ENSP00000216361.5:p.Lys580Asn
ENST00000396618.9:c.1545A>C MANE Select ENSP00000379862.3:p.Lys515Asn
ENST00000555117.2:c.1534+3371A>C ENSP00000493569.1:n.1534+3371A>C
ENST00000643575.1:c.1545A>C ENSP00000494838.1:p.Lys515Asn
ENST00000643697.1:n.1847A>C
ENST00000644874.2:c.1545A>C ENSP00000496360.1:p.Lys515Asn
ENST00000216361.8:c.1545A>C ENSP00000216361.4:p.Lys515Asn
ENST00000396618.7:c.1545A>C ENSP00000379862.3:p.Lys515Asn
ENST00000460581.6:c.1209A>C ENSP00000451713.1:p.Lys403Asn
ENST00000468826.2:c.1196A>C
ENST00000475087.5:c.1477+3371A>C ENSP00000451528.1:n.1477+3371A>C
NM_001135058.1:c.1545A>C NP_001128530.1:p.Lys515Asn
NM_004086.2:c.1545A>C NP_004077.1:p.Lys515Asn
NR_038356.1:n.126T>G
XM_011536539.1:c.1545A>C XP_011534841.1:p.Lys515Asn
NM_001347720.1:c.1740A>C NP_001334649.1:p.Lys580Asn
XM_017021071.1:c.1740A>C XP_016876560.1:p.Lys580Asn
XM_024449506.1:c.1602A>C XP_024305274.1:p.Lys534Asn
NM_004086.3:c.1545A>C MANE Select NP_004077.1:p.Lys515Asn
NM_001135058.2:c.1545A>C NP_001128530.1:p.Lys515Asn
NM_001347720.2:c.1740A>C NP_001334649.1:p.Lys580Asn