Canonical Allele Identifier: CA2126957374

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885392_30885403delinsAGGAAAAGCCTT , CM000676.2:g.30885392_30885403delinsAGGAAAAGCCTT	GRCh38
NC_000014.8:g.31354598_31354609delinsAGGAAAAGCCTT , CM000676.1:g.31354598_31354609delinsAGGAAAAGCCTT	GRCh37
NC_000014.7:g.30424349_30424360delinsAGGAAAAGCCTT	NCBI36
NG_008211.2:g.15858_15869delinsAGGAAAAGCCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000216361.9:c.929-2_938delinsAGGAAAAGCCTT
ENST00000396618.9:c.734-2_743delinsAGGAAAAGCCTT
ENST00000555117.2:c.791-2_800delinsAGGAAAAGCCTT
ENST00000643575.1:c.734-2_743delinsAGGAAAAGCCTT
ENST00000643697.1:n.1036-2_1045delinsAGGAAAAGCCTT
ENST00000644874.2:c.734-2_743delinsAGGAAAAGCCTT
ENST00000216361.8:c.734-2_743delinsAGGAAAAGCCTT
ENST00000396618.7:c.734-2_743delinsAGGAAAAGCCTT
ENST00000460581.6:c.398-2_407delinsAGGAAAAGCCTT
ENST00000468826.2:c.385-2_394delinsAGGAAAAGCCTT
ENST00000475087.5:c.734-2_743delinsAGGAAAAGCCTT
ENST00000555881.5:c.380-2_389delinsAGGAAAAGCCTT
ENST00000557065.1:c.516-2_525delinsAGGAAAAGCCTT
NM_001135058.1:c.734-2_743delinsAGGAAAAGCCTT
NM_004086.2:c.734-2_743delinsAGGAAAAGCCTT
NR_038356.1:n.1452+10_1452+21delinsAAGGCTTTTCCT
XM_011536539.1:c.734-2_743delinsAGGAAAAGCCTT
NM_001347720.1:c.929-2_938delinsAGGAAAAGCCTT
XM_017021071.1:c.929-2_938delinsAGGAAAAGCCTT
XM_024449506.1:c.791-2_800delinsAGGAAAAGCCTT
NM_004086.3:c.734-2_743delinsAGGAAAAGCCTT
NM_001135058.2:c.734-2_743delinsAGGAAAAGCCTT
NM_001347720.2:c.929-2_938delinsAGGAAAAGCCTT