Canonical Allele Identifier: CA613199
Community Standard Title: NM_007272.3(CTRC):c.46A>G (p.Ser16Gly)
Gene: CTRC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440305A>G , CM000663.2:g.15440305A>G GRCh38
NC_000001.10:g.15766801A>G , CM000663.1:g.15766801A>G GRCh37
NC_000001.9:g.15639388A>G NCBI36
NG_009253.1:g.6864A>G

Transcript Alleles

HGVS Amino-acid Change
NM_007272.3:c.46A>G MANE Select NP_009203.2:p.Ser16Gly
ENST00000375949.5:c.46A>G MANE Select ENSP00000365116.4:p.Ser16Gly
NM_007272.2:c.46A>G NP_009203.2:p.Ser16Gly
ENST00000375943.6:c.40+1801A>G ENSP00000365110.2:n.40+1801A>G
ENST00000375949.4:c.46A>G ENSP00000365116.4:p.Ser16Gly
ENST00000476813.5:n.52+1801A>G
XM_011540550.1:c.46A>G XP_011538852.1:p.Ser16Gly
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