Canonical Allele Identifier: CA2624446787

Gene: COCH

Linked Data

• gnomAD v4: 14-30890230-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30890230G>T , CM000676.2:g.30890230G>T	GRCh38
NC_000014.8:g.31359436G>T , CM000676.1:g.31359436G>T	GRCh37
NC_000014.7:g.30429187G>T	NCBI36
NG_008211.2:g.20696G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396618.9:c.*439G>T MANE Select	ENSP00000379862.3:n.*439G>T
ENST00000555117.2:c.1534+3918G>T	ENSP00000493569.1:n.1534+3918G>T
ENST00000643575.1:c.*2+437G>T	ENSP00000494838.1:n.*2+437G>T
ENST00000644874.2:c.*439G>T	ENSP00000496360.1:n.*439G>T
ENST00000396618.7:c.*439G>T	ENSP00000379862.3:n.*439G>T
ENST00000460581.6:c.*439G>T	ENSP00000451713.1:n.*439G>T
ENST00000468826.2:c.1743G>T
ENST00000475087.5:c.1477+3918G>T	ENSP00000451528.1:n.1477+3918G>T
NM_001135058.1:c.*439G>T	NP_001128530.1:n.*439G>T
NM_004086.2:c.*439G>T	NP_004077.1:n.*439G>T
XM_011536539.1:c.*2+437G>T	XP_011534841.1:n.*2+437G>T
NM_001347720.1:c.*439G>T	NP_001334649.1:n.*439G>T
XM_017021071.1:c.*439G>T	XP_016876560.1:n.*439G>T
XM_024449506.1:c.*439G>T	XP_024305274.1:n.*439G>T
NM_004086.3:c.*439G>T MANE Select	NP_004077.1:n.*439G>T
NM_001135058.2:c.*439G>T	NP_001128530.1:n.*439G>T
NM_001347720.2:c.*439G>T	NP_001334649.1:n.*439G>T