Canonical Allele Identifier: CA613470
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs777187660
ExAC: 1:15772232 C / G
gnomAD v2: 1-15772232-C-G
MyVariant Identifiers: chr1:g.15772232C>G (hg19) chr1:g.15445737C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445737C>G , CM000663.2:g.15445737C>G GRCh38
NC_000001.10:g.15772232C>G , CM000663.1:g.15772232C>G GRCh37
NC_000001.9:g.15644819C>G NCBI36
NG_009253.1:g.12295C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.780C>G MANE Select ENSP00000365116.4:p.Asp260Glu
ENST00000375943.6:c.*234C>G ENSP00000365110.2:n.*234C>G
ENST00000375949.4:c.780C>G ENSP00000365116.4:p.Asp260Glu
ENST00000483406.1:n.544C>G
NM_007272.2:c.780C>G NP_009203.2:p.Asp260Glu
XM_011540550.1:c.634C>G XP_011538852.1:p.Leu212Val
NM_007272.3:c.780C>G MANE Select NP_009203.2:p.Asp260Glu
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