Canonical Allele Identifier: CA2643487254

Gene: CTRC

Linked Data

• gnomAD v4: 1-15440478-CCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15440481_15440483del , CM000663.2:g.15440481_15440483del	GRCh38
NC_000001.10:g.15766977_15766979del , CM000663.1:g.15766977_15766979del	GRCh37
NC_000001.9:g.15639564_15639566del	NCBI36
NG_009253.1:g.7040_7042del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.133-12_133-10del MANE Select	ENSP00000365116.4:n.133-12_133-10del
ENST00000375943.6:c.41-1966_41-1964del	ENSP00000365110.2:n.41-1966_41-1964del
ENST00000375949.4:c.133-12_133-10del	ENSP00000365116.4:n.133-12_133-10del
ENST00000476813.5:n.53-1966_53-1964del
ENST00000483406.1:n.43-12_43-10del
NM_007272.2:c.133-12_133-10del	NP_009203.2:n.133-12_133-10del
XM_011540550.1:c.133-12_133-10del	XP_011538852.1:n.133-12_133-10del
NM_007272.3:c.133-12_133-10del MANE Select	NP_009203.2:n.133-12_133-10del