Canonical Allele Identifier: CA389344718

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31348124G>C (hg19) ; chr14:g.30878918G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30878918G>C , CM000676.2:g.30878918G>C	GRCh38
NC_000014.8:g.31348124G>C , CM000676.1:g.31348124G>C	GRCh37
NC_000014.7:g.30417875G>C	NCBI36
NG_008211.2:g.9384G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.542G>C	ENSP00000216361.5:p.Arg181Thr
ENST00000396618.9:c.347G>C MANE Select	ENSP00000379862.3:p.Arg116Thr
ENST00000555117.2:c.347G>C	ENSP00000493569.1:p.Arg116Thr
ENST00000643575.1:c.347G>C	ENSP00000494838.1:p.Arg116Thr
ENST00000643697.1:n.592G>C
ENST00000644874.2:c.347G>C	ENSP00000496360.1:p.Arg116Thr
ENST00000216361.8:c.347G>C	ENSP00000216361.4:p.Arg116Thr
ENST00000396618.7:c.347G>C	ENSP00000379862.3:p.Arg116Thr
ENST00000460581.6:c.11G>C	ENSP00000451713.1:p.Arg4Thr
ENST00000475087.5:c.347G>C	ENSP00000451528.1:p.Arg116Thr
ENST00000553772.5:c.239+1190G>C	ENSP00000452343.1:n.239+1190G>C
ENST00000553833.5:n.501G>C
ENST00000555881.5:c.83-1534G>C	ENSP00000452569.1:n.83-1534G>C
ENST00000556908.5:c.299G>C	ENSP00000452541.1:p.Arg100Thr
ENST00000557065.1:c.156-505G>C	ENSP00000451629.1:n.156-505G>C
NM_001135058.1:c.347G>C	NP_001128530.1:p.Arg116Thr
NM_004086.2:c.347G>C	NP_004077.1:p.Arg116Thr
NR_038356.1:n.1618-2366C>G
XM_011536539.1:c.347G>C	XP_011534841.1:p.Arg116Thr
NM_001347720.1:c.542G>C	NP_001334649.1:p.Arg181Thr
XM_017021071.1:c.542G>C	XP_016876560.1:p.Arg181Thr
XM_024449506.1:c.347G>C	XP_024305274.1:p.Arg116Thr
NM_004086.3:c.347G>C MANE Select	NP_004077.1:p.Arg116Thr
NM_001135058.2:c.347G>C	NP_001128530.1:p.Arg116Thr
NM_001347720.2:c.542G>C	NP_001334649.1:p.Arg181Thr