Canonical Allele Identifier: CA1155328418
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445560G= , CM000663.2:g.15445560G= GRCh38
NC_000001.10:g.15772055G= , CM000663.1:g.15772055G= GRCh37
NC_000001.9:g.15644642G= NCBI36
NG_009253.1:g.12118G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-37G= MANE Select ENSP00000365116.4:n.640-37G=
ENST00000375943.6:c.*94-37G= ENSP00000365110.2:n.*94-37G=
ENST00000375949.4:c.640-37G= ENSP00000365116.4:n.640-37G=
ENST00000483406.1:n.404-37G=
NM_007272.2:c.640-37G= NP_009203.2:n.640-37G=
XM_011540550.1:c.494-37G= XP_011538852.1:n.494-37G=
NM_007272.3:c.640-37G= MANE Select NP_009203.2:n.640-37G=