Canonical Allele Identifier: CA2643487310
Gene: CTRC HGNC NCBI

Linked Data

gnomAD v4: 1-15445826-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445826T>A , CM000663.2:g.15445826T>A GRCh38
NC_000001.10:g.15772321T>A , CM000663.1:g.15772321T>A GRCh37
NC_000001.9:g.15644908T>A NCBI36
NG_009253.1:g.12384T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+77T>A MANE Select ENSP00000365116.4:n.792+77T>A
ENST00000375943.6:c.*246+77T>A ENSP00000365110.2:n.*246+77T>A
ENST00000375949.4:c.792+77T>A ENSP00000365116.4:n.792+77T>A
ENST00000483406.1:n.556+77T>A
NM_007272.2:c.792+77T>A NP_009203.2:n.792+77T>A
XM_011540550.1:c.646+77T>A XP_011538852.1:n.646+77T>A
NM_007272.3:c.792+77T>A MANE Select NP_009203.2:n.792+77T>A
Search 100 bp 5'
Search 100 bp 3'