Canonical Allele Identifier: CA389348445

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31355216A>G (hg19) ; chr14:g.30886010A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30886010A>G , CM000676.2:g.30886010A>G	GRCh38
NC_000014.8:g.31355216A>G , CM000676.1:g.31355216A>G	GRCh37
NC_000014.7:g.30424967A>G	NCBI36
NG_008211.2:g.16476A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1370A>G	ENSP00000216361.5:p.Asn457Ser
ENST00000396618.9:c.1175A>G MANE Select	ENSP00000379862.3:p.Asn392Ser
ENST00000555117.2:c.1232A>G	ENSP00000493569.1:p.Asn411Ser
ENST00000643575.1:c.1175A>G	ENSP00000494838.1:p.Asn392Ser
ENST00000643697.1:n.1477A>G
ENST00000644874.2:c.1175A>G	ENSP00000496360.1:p.Asn392Ser
ENST00000216361.8:c.1175A>G	ENSP00000216361.4:p.Asn392Ser
ENST00000396618.7:c.1175A>G	ENSP00000379862.3:p.Asn392Ser
ENST00000460581.6:c.839A>G	ENSP00000451713.1:p.Asn280Ser
ENST00000468826.2:c.826A>G
ENST00000475087.5:c.1175A>G	ENSP00000451528.1:p.Asn392Ser
NM_001135058.1:c.1175A>G	NP_001128530.1:p.Asn392Ser
NM_004086.2:c.1175A>G	NP_004077.1:p.Asn392Ser
NR_038356.1:n.855T>C
XM_011536539.1:c.1175A>G	XP_011534841.1:p.Asn392Ser
NM_001347720.1:c.1370A>G	NP_001334649.1:p.Asn457Ser
XM_017021071.1:c.1370A>G	XP_016876560.1:p.Asn457Ser
XM_024449506.1:c.1232A>G	XP_024305274.1:p.Asn411Ser
NM_004086.3:c.1175A>G MANE Select	NP_004077.1:p.Asn392Ser
NM_001135058.2:c.1175A>G	NP_001128530.1:p.Asn392Ser
NM_001347720.2:c.1370A>G	NP_001334649.1:p.Asn457Ser