Canonical Allele Identifier: CA485829832

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31348690A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30879484A>G , CM000676.2:g.30879484A>G	GRCh38
NC_000014.8:g.31348690A>G , CM000676.1:g.31348690A>G	GRCh37
NC_000014.7:g.30418441A>G	NCBI36
NG_008211.2:g.9950A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.630A>G	ENSP00000216361.5:p.Thr210=
ENST00000396618.9:c.435A>G MANE Select	ENSP00000379862.3:p.Thr145=
ENST00000555117.2:c.435A>G	ENSP00000493569.1:p.Thr145=
ENST00000643575.1:c.435A>G	ENSP00000494838.1:p.Thr145=
ENST00000643697.1:n.680A>G
ENST00000644874.2:c.435A>G	ENSP00000496360.1:p.Thr145=
ENST00000216361.8:c.435A>G	ENSP00000216361.4:p.Thr145=
ENST00000396618.7:c.435A>G	ENSP00000379862.3:p.Thr145=
ENST00000460581.6:c.99A>G	ENSP00000451713.1:p.Thr33=
ENST00000475087.5:c.435A>G	ENSP00000451528.1:p.Thr145=
ENST00000553772.5:c.240-968A>G	ENSP00000452343.1:n.240-968A>G
ENST00000553833.5:n.589A>G
ENST00000555881.5:c.83-968A>G	ENSP00000452569.1:n.83-968A>G
ENST00000556908.5:c.387A>G	ENSP00000452541.1:p.Thr129=
ENST00000557065.1:c.217A>G	ENSP00000451629.1:n.217A>G
NM_001135058.1:c.435A>G	NP_001128530.1:p.Thr145=
NM_004086.2:c.435A>G	NP_004077.1:p.Thr145=
NR_038356.1:n.1618-2932T>C
XM_011536539.1:c.435A>G	XP_011534841.1:p.Thr145=
NM_001347720.1:c.630A>G	NP_001334649.1:p.Thr210=
XM_017021071.1:c.630A>G	XP_016876560.1:p.Thr210=
XM_024449506.1:c.435A>G	XP_024305274.1:p.Thr145=
NM_004086.3:c.435A>G MANE Select	NP_004077.1:p.Thr145=
NM_001135058.2:c.435A>G	NP_001128530.1:p.Thr145=
NM_001347720.2:c.630A>G	NP_001334649.1:p.Thr210=