Canonical Allele Identifier: CA1155329104

Gene: CTRC

Linked Data

• dbSNP Id: rs1708212947

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445930_15445933del , CM000663.2:g.15445930_15445933del	GRCh38
NC_000001.10:g.15772425_15772428del , CM000663.1:g.15772425_15772428del	GRCh37
NC_000001.9:g.15645012_15645015del	NCBI36
NG_009253.1:g.12488_12491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+181_792+184del MANE Select	ENSP00000365116.4:n.792+181_792+184del
ENST00000375943.6:c.*246+181_*246+184del	ENSP00000365110.2:n.*246+181_*246+184del
ENST00000375949.4:c.792+181_792+184del	ENSP00000365116.4:n.792+181_792+184del
ENST00000483406.1:n.556+181_556+184del
NM_007272.2:c.792+181_792+184del	NP_009203.2:n.792+181_792+184del
XM_011540550.1:c.646+181_646+184del	XP_011538852.1:n.646+181_646+184del
NM_007272.3:c.792+181_792+184del MANE Select	NP_009203.2:n.792+181_792+184del