Canonical Allele Identifier: CA2643487134
Gene: CTRC HGNC NCBI

Linked Data

gnomAD v4: 1-15445485-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445485A>T , CM000663.2:g.15445485A>T GRCh38
NC_000001.10:g.15771980A>T , CM000663.1:g.15771980A>T GRCh37
NC_000001.9:g.15644567A>T NCBI36
NG_009253.1:g.12043A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-112A>T MANE Select ENSP00000365116.4:n.640-112A>T
ENST00000375943.6:c.*94-112A>T ENSP00000365110.2:n.*94-112A>T
ENST00000375949.4:c.640-112A>T ENSP00000365116.4:n.640-112A>T
ENST00000483406.1:n.404-112A>T
NM_007272.2:c.640-112A>T NP_009203.2:n.640-112A>T
XM_011540550.1:c.494-112A>T XP_011538852.1:n.494-112A>T
NM_007272.3:c.640-112A>T MANE Select NP_009203.2:n.640-112A>T
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