Canonical Allele Identifier: CA389348116
Gene: COCH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30885865A>C , CM000676.2:g.30885865A>C GRCh38
NC_000014.8:g.31355071A>C , CM000676.1:g.31355071A>C GRCh37
NC_000014.7:g.30424822A>C NCBI36
NG_008211.2:g.16331A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216361.9:c.1225A>C ENSP00000216361.5:p.Lys409Gln
ENST00000396618.9:c.1030A>C MANE Select ENSP00000379862.3:p.Lys344Gln
ENST00000555117.2:c.1087A>C ENSP00000493569.1:p.Lys363Gln
ENST00000643575.1:c.1030A>C ENSP00000494838.1:p.Lys344Gln
ENST00000643697.1:n.1332A>C
ENST00000644874.2:c.1030A>C ENSP00000496360.1:p.Lys344Gln
ENST00000216361.8:c.1030A>C ENSP00000216361.4:p.Lys344Gln
ENST00000396618.7:c.1030A>C ENSP00000379862.3:p.Lys344Gln
ENST00000460581.6:c.694A>C ENSP00000451713.1:p.Lys232Gln
ENST00000468826.2:c.681A>C
ENST00000475087.5:c.1030A>C ENSP00000451528.1:p.Lys344Gln
NM_001135058.1:c.1030A>C NP_001128530.1:p.Lys344Gln
NM_004086.2:c.1030A>C NP_004077.1:p.Lys344Gln
NR_038356.1:n.1000T>G
XM_011536539.1:c.1030A>C XP_011534841.1:p.Lys344Gln
NM_001347720.1:c.1225A>C NP_001334649.1:p.Lys409Gln
XM_017021071.1:c.1225A>C XP_016876560.1:p.Lys409Gln
XM_024449506.1:c.1087A>C XP_024305274.1:p.Lys363Gln
NM_004086.3:c.1030A>C MANE Select NP_004077.1:p.Lys344Gln
NM_001135058.2:c.1030A>C NP_001128530.1:p.Lys344Gln
NM_001347720.2:c.1225A>C NP_001334649.1:p.Lys409Gln