Canonical Allele Identifier: CA485832206

Gene: COCH

Linked Data

• dbSNP Id: rs1406717795
• MyVariant Identifiers: chr14:g.31354622T>C (hg19) ; chr14:g.30885416T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885416T>C , CM000676.2:g.30885416T>C	GRCh38
NC_000014.8:g.31354622T>C , CM000676.1:g.31354622T>C	GRCh37
NC_000014.7:g.30424373T>C	NCBI36
NG_008211.2:g.15882T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.951T>C	ENSP00000216361.5:p.Ala317=
ENST00000396618.9:c.756T>C MANE Select	ENSP00000379862.3:p.Ala252=
ENST00000555117.2:c.813T>C	ENSP00000493569.1:p.Ala271=
ENST00000643575.1:c.756T>C	ENSP00000494838.1:p.Ala252=
ENST00000643697.1:n.1058T>C
ENST00000644874.2:c.756T>C	ENSP00000496360.1:p.Ala252=
ENST00000216361.8:c.756T>C	ENSP00000216361.4:p.Ala252=
ENST00000396618.7:c.756T>C	ENSP00000379862.3:p.Ala252=
ENST00000460581.6:c.420T>C	ENSP00000451713.1:p.Ala140=
ENST00000468826.2:c.407T>C
ENST00000475087.5:c.756T>C	ENSP00000451528.1:p.Ala252=
ENST00000555881.5:c.402T>C	ENSP00000452569.1:p.Ala134=
ENST00000557065.1:c.538T>C	ENSP00000451629.1:n.538T>C
NM_001135058.1:c.756T>C	NP_001128530.1:p.Ala252=
NM_004086.2:c.756T>C	NP_004077.1:p.Ala252=
NR_038356.1:n.1449A>G
XM_011536539.1:c.756T>C	XP_011534841.1:p.Ala252=
NM_001347720.1:c.951T>C	NP_001334649.1:p.Ala317=
XM_017021071.1:c.951T>C	XP_016876560.1:p.Ala317=
XM_024449506.1:c.813T>C	XP_024305274.1:p.Ala271=
NM_004086.3:c.756T>C MANE Select	NP_004077.1:p.Ala252=
NM_001135058.2:c.756T>C	NP_001128530.1:p.Ala252=
NM_001347720.2:c.951T>C	NP_001334649.1:p.Ala317=