Canonical Allele Identifier: CA2126960749
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30889673T= , CM000676.2:g.30889673T= GRCh38
NC_000014.8:g.31358879T= , CM000676.1:g.31358879T= GRCh37
NC_000014.7:g.30428630T= NCBI36
NG_008211.2:g.20139T=

Transcript Alleles

HGVS Amino-acid change
ENST00000216361.9:c.1730T= ENSP00000216361.5:p.Met577=
ENST00000396618.9:c.1535T= MANE Select ENSP00000379862.3:p.Met512=
ENST00000555117.2:c.1534+3361T= ENSP00000493569.1:n.1534+3361T=
ENST00000643575.1:c.1535T= ENSP00000494838.1:p.Met512=
ENST00000643697.1:n.1837T=
ENST00000644874.2:c.1535T= ENSP00000496360.1:p.Met512=
ENST00000216361.8:c.1535T= ENSP00000216361.4:p.Met512=
ENST00000396618.7:c.1535T= ENSP00000379862.3:p.Met512=
ENST00000460581.6:c.1199T= ENSP00000451713.1:p.Met400=
ENST00000468826.2:c.1186T=
ENST00000475087.5:c.1477+3361T= ENSP00000451528.1:n.1477+3361T=
NM_001135058.1:c.1535T= NP_001128530.1:p.Met512=
NM_004086.2:c.1535T= NP_004077.1:p.Met512=
NR_038356.1:n.136A=
XM_011536539.1:c.1535T= XP_011534841.1:p.Met512=
NM_001347720.1:c.1730T= NP_001334649.1:p.Met577=
XM_017021071.1:c.1730T= XP_016876560.1:p.Met577=
XM_024449506.1:c.1592T= XP_024305274.1:p.Met531=
NM_004086.3:c.1535T= MANE Select NP_004077.1:p.Met512=
NM_001135058.2:c.1535T= NP_001128530.1:p.Met512=
NM_001347720.2:c.1730T= NP_001334649.1:p.Met577=