Canonical Allele Identifier: CA2643487265

Gene: CTRC

Linked Data

• gnomAD v4: 1-15445726-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445728del , CM000663.2:g.15445728del	GRCh38
NC_000001.10:g.15772223del , CM000663.1:g.15772223del	GRCh37
NC_000001.9:g.15644810del	NCBI36
NG_009253.1:g.12286del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375949.5:c.771del MANE Select	ENSP00000365116.4:p.Tyr258ThrfsTer?
ENST00000375943.6:c.*225del	ENSP00000365110.2:n.*225del
ENST00000375949.4:c.771del	ENSP00000365116.4:p.Tyr258ThrfsTer?
ENST00000483406.1:n.535del
NM_007272.2:c.771del	NP_009203.2:p.Tyr258ThrfsTer?
XM_011540550.1:c.625del	XP_011538852.1:p.Leu209TyrfsTer12
NM_007272.3:c.771del MANE Select	NP_009203.2:p.Tyr258ThrfsTer?