Canonical Allele Identifier: CA2643487221
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445556_15445557insA , CM000663.2:g.15445556_15445557insA GRCh38
NC_000001.10:g.15772051_15772052insA , CM000663.1:g.15772051_15772052insA GRCh37
NC_000001.9:g.15644638_15644639insA NCBI36
NG_009253.1:g.12114_12115insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-41_640-40insA MANE Select ENSP00000365116.4:n.640-41_640-40insA
ENST00000375943.6:c.*94-41_*94-40insA ENSP00000365110.2:n.*94-41_*94-40insA
ENST00000375949.4:c.640-41_640-40insA ENSP00000365116.4:n.640-41_640-40insA
ENST00000483406.1:n.404-41_404-40insA
NM_007272.2:c.640-41_640-40insA NP_009203.2:n.640-41_640-40insA
XM_011540550.1:c.494-41_494-40insA XP_011538852.1:n.494-41_494-40insA
NM_007272.3:c.640-41_640-40insA MANE Select NP_009203.2:n.640-41_640-40insA