Canonical Allele Identifier: CA1155328657

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445687_15445711delinsAACACCCGCAAGAAGCCGGTAGTCT , CM000663.2:g.15445687_15445711delinsAACACCCGCAAGAAGCCGGTAGTCT	GRCh38
NC_000001.10:g.15772182_15772206delinsAACACCCGCAAGAAGCCGGTAGTCT , CM000663.1:g.15772182_15772206delinsAACACCCGCAAGAAGCCGGTAGTCT	GRCh37
NC_000001.9:g.15644769_15644793delinsAACACCCGCAAGAAGCCGGTAGTCT	NCBI36
NG_009253.1:g.12245_12269delinsAACACCCGCAAGAAGCCGGTAGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.730_754delinsAACACCCGCAAGAAGCCGGTAGTCT MANE Select	ENSP00000365116.4:p.Asn244=
ENST00000375943.6:c.*184_*208delinsAACACCCGCAAGAAGCCGGTAGTCT	ENSP00000365110.2:n.*184_*208delinsAACACCCGCAAGAAGCCGGTAGTCT
ENST00000375949.4:c.730_754delinsAACACCCGCAAGAAGCCGGTAGTCT	ENSP00000365116.4:p.Asn244=
ENST00000483406.1:n.494_518delinsAACACCCGCAAGAAGCCGGTAGTCT
NM_007272.2:c.730_754delinsAACACCCGCAAGAAGCCGGTAGTCT	NP_009203.2:p.Asn244=
XM_011540550.1:c.584_608delinsAACACCCGCAAGAAGCCGGTAGTCT	XP_011538852.1:p.Gln195=
NM_007272.3:c.730_754delinsAACACCCGCAAGAAGCCGGTAGTCT MANE Select	NP_009203.2:p.Asn244=