Canonical Allele Identifier: CA1146210716
Gene: CTRC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445526A= , CM000663.2:g.15445526A= GRCh38
NC_000001.10:g.15772021A= , CM000663.1:g.15772021A= GRCh37
NC_000001.9:g.15644608A= NCBI36
NG_009253.1:g.12084A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-71A= MANE Select ENSP00000365116.4:n.640-71A=
ENST00000375943.6:c.*94-71A= ENSP00000365110.2:n.*94-71A=
ENST00000375949.4:c.640-71A= ENSP00000365116.4:n.640-71A=
ENST00000483406.1:n.404-71A=
NM_007272.2:c.640-71A= NP_009203.2:n.640-71A=
XM_011540550.1:c.494-71A= XP_011538852.1:n.494-71A=
NM_007272.3:c.640-71A= MANE Select NP_009203.2:n.640-71A=
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