Canonical Allele Identifier: CA416207343
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772103T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445608T>G , CM000663.2:g.15445608T>G GRCh38
NC_000001.10:g.15772103T>G , CM000663.1:g.15772103T>G GRCh37
NC_000001.9:g.15644690T>G NCBI36
NG_009253.1:g.12166T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.651T>G MANE Select ENSP00000365116.4:p.Gly217=
ENST00000375943.6:c.*105T>G ENSP00000365110.2:n.*105T>G
ENST00000375949.4:c.651T>G ENSP00000365116.4:p.Gly217=
ENST00000483406.1:n.415T>G
NM_007272.2:c.651T>G NP_009203.2:p.Gly217=
XM_011540550.1:c.505T>G XP_011538852.1:p.Trp169Gly
NM_007272.3:c.651T>G MANE Select NP_009203.2:p.Gly217=