Canonical Allele Identifier: CA2575499999

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885370del , CM000676.2:g.30885370del	GRCh38
NC_000014.8:g.31354576del , CM000676.1:g.31354576del	GRCh37
NC_000014.7:g.30424327del	NCBI36
NG_008211.2:g.15836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.929-24del	ENSP00000216361.5:n.929-24del
ENST00000396618.9:c.734-24del MANE Select	ENSP00000379862.3:n.734-24del
ENST00000555117.2:c.791-24del	ENSP00000493569.1:n.791-24del
ENST00000643575.1:c.734-24del	ENSP00000494838.1:n.734-24del
ENST00000643697.1:n.1036-24del
ENST00000644874.2:c.734-24del	ENSP00000496360.1:n.734-24del
ENST00000216361.8:c.734-24del	ENSP00000216361.4:n.734-24del
ENST00000396618.7:c.734-24del	ENSP00000379862.3:n.734-24del
ENST00000460581.6:c.398-24del	ENSP00000451713.1:n.398-24del
ENST00000468826.2:c.385-24del
ENST00000475087.5:c.734-24del	ENSP00000451528.1:n.734-24del
ENST00000555881.5:c.380-24del	ENSP00000452569.1:n.380-24del
ENST00000557065.1:c.516-24del	ENSP00000451629.1:n.516-24del
NM_001135058.1:c.734-24del	NP_001128530.1:n.734-24del
NM_004086.2:c.734-24del	NP_004077.1:n.734-24del
NR_038356.1:n.1452+45del
XM_011536539.1:c.734-24del	XP_011534841.1:n.734-24del
NM_001347720.1:c.929-24del	NP_001334649.1:n.929-24del
XM_017021071.1:c.929-24del	XP_016876560.1:n.929-24del
XM_024449506.1:c.791-24del	XP_024305274.1:n.791-24del
NM_004086.3:c.734-24del MANE Select	NP_004077.1:n.734-24del
NM_001135058.2:c.734-24del	NP_001128530.1:n.734-24del
NM_001347720.2:c.929-24del	NP_001334649.1:n.929-24del