Canonical Allele Identifier: CA389348553

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31355267T>C (hg19) ; chr14:g.30886061T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30886061T>C , CM000676.2:g.30886061T>C	GRCh38
NC_000014.8:g.31355267T>C , CM000676.1:g.31355267T>C	GRCh37
NC_000014.7:g.30425018T>C	NCBI36
NG_008211.2:g.16527T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1421T>C	ENSP00000216361.5:p.Val474Ala
ENST00000396618.9:c.1226T>C MANE Select	ENSP00000379862.3:p.Val409Ala
ENST00000555117.2:c.1283T>C	ENSP00000493569.1:p.Val428Ala
ENST00000643575.1:c.1226T>C	ENSP00000494838.1:p.Val409Ala
ENST00000643697.1:n.1528T>C
ENST00000644874.2:c.1226T>C	ENSP00000496360.1:p.Val409Ala
ENST00000216361.8:c.1226T>C	ENSP00000216361.4:p.Val409Ala
ENST00000396618.7:c.1226T>C	ENSP00000379862.3:p.Val409Ala
ENST00000460581.6:c.890T>C	ENSP00000451713.1:p.Val297Ala
ENST00000468826.2:c.877T>C
ENST00000475087.5:c.1226T>C	ENSP00000451528.1:p.Val409Ala
NM_001135058.1:c.1226T>C	NP_001128530.1:p.Val409Ala
NM_004086.2:c.1226T>C	NP_004077.1:p.Val409Ala
NR_038356.1:n.804A>G
XM_011536539.1:c.1226T>C	XP_011534841.1:p.Val409Ala
NM_001347720.1:c.1421T>C	NP_001334649.1:p.Val474Ala
XM_017021071.1:c.1421T>C	XP_016876560.1:p.Val474Ala
XM_024449506.1:c.1283T>C	XP_024305274.1:p.Val428Ala
NM_004086.3:c.1226T>C MANE Select	NP_004077.1:p.Val409Ala
NM_001135058.2:c.1226T>C	NP_001128530.1:p.Val409Ala
NM_001347720.2:c.1421T>C	NP_001334649.1:p.Val474Ala