Canonical Allele Identifier: CA389344706

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31348118T>A (hg19) ; chr14:g.30878912T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30878912T>A , CM000676.2:g.30878912T>A	GRCh38
NC_000014.8:g.31348118T>A , CM000676.1:g.31348118T>A	GRCh37
NC_000014.7:g.30417869T>A	NCBI36
NG_008211.2:g.9378T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.536T>A	ENSP00000216361.5:p.Leu179His
ENST00000396618.9:c.341T>A MANE Select	ENSP00000379862.3:p.Leu114His
ENST00000555117.2:c.341T>A	ENSP00000493569.1:p.Leu114His
ENST00000643575.1:c.341T>A	ENSP00000494838.1:p.Leu114His
ENST00000643697.1:n.586T>A
ENST00000644874.2:c.341T>A	ENSP00000496360.1:p.Leu114His
ENST00000216361.8:c.341T>A	ENSP00000216361.4:p.Leu114His
ENST00000396618.7:c.341T>A	ENSP00000379862.3:p.Leu114His
ENST00000460581.6:c.5T>A	ENSP00000451713.1:p.Leu2His
ENST00000475087.5:c.341T>A	ENSP00000451528.1:p.Leu114His
ENST00000553772.5:c.239+1184T>A	ENSP00000452343.1:n.239+1184T>A
ENST00000553833.5:n.495T>A
ENST00000555881.5:c.83-1540T>A	ENSP00000452569.1:n.83-1540T>A
ENST00000556908.5:c.293T>A	ENSP00000452541.1:p.Leu98His
ENST00000557065.1:c.156-511T>A	ENSP00000451629.1:n.156-511T>A
NM_001135058.1:c.341T>A	NP_001128530.1:p.Leu114His
NM_004086.2:c.341T>A	NP_004077.1:p.Leu114His
NR_038356.1:n.1618-2360A>T
XM_011536539.1:c.341T>A	XP_011534841.1:p.Leu114His
NM_001347720.1:c.536T>A	NP_001334649.1:p.Leu179His
XM_017021071.1:c.536T>A	XP_016876560.1:p.Leu179His
XM_024449506.1:c.341T>A	XP_024305274.1:p.Leu114His
NM_004086.3:c.341T>A MANE Select	NP_004077.1:p.Leu114His
NM_001135058.2:c.341T>A	NP_001128530.1:p.Leu114His
NM_001347720.2:c.536T>A	NP_001334649.1:p.Leu179His