Canonical Allele Identifier: CA18254162

Gene: CTRC

Linked Data

• dbSNP Id: rs142877180
• MyVariant Identifiers: chr1:g.15772502_15772503insCATT (hg19) ; chr1:g.15446007_15446008insCATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15446007_15446008insCATT , CM000663.2:g.15446007_15446008insCATT	GRCh38
NC_000001.10:g.15772502_15772503insCATT , CM000663.1:g.15772502_15772503insCATT	GRCh37
NC_000001.9:g.15645089_15645090insCATT	NCBI36
NG_009253.1:g.12565_12566insCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+258_792+259insCATT MANE Select	ENSP00000365116.4:n.792+258_792+259insCATT
ENST00000375943.6:c.*246+258_*246+259insCATT	ENSP00000365110.2:n.*246+258_*246+259insCATT
ENST00000375949.4:c.792+258_792+259insCATT	ENSP00000365116.4:n.792+258_792+259insCATT
ENST00000483406.1:n.556+258_556+259insCATT
NM_007272.2:c.792+258_792+259insCATT	NP_009203.2:n.792+258_792+259insCATT
XM_011540550.1:c.646+258_646+259insCATT	XP_011538852.1:n.646+258_646+259insCATT
NM_007272.3:c.792+258_792+259insCATT MANE Select	NP_009203.2:n.792+258_792+259insCATT