Canonical Allele Identifier: CA338567749
Gene: CTRC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.15772129A>G (hg19) chr1:g.15445634A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445634A>G , CM000663.2:g.15445634A>G GRCh38
NC_000001.10:g.15772129A>G , CM000663.1:g.15772129A>G GRCh37
NC_000001.9:g.15644716A>G NCBI36
NG_009253.1:g.12192A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.677A>G MANE Select ENSP00000365116.4:p.Asn226Ser
ENST00000375943.6:c.*131A>G ENSP00000365110.2:n.*131A>G
ENST00000375949.4:c.677A>G ENSP00000365116.4:p.Asn226Ser
ENST00000483406.1:n.441A>G
NM_007272.2:c.677A>G NP_009203.2:p.Asn226Ser
XM_011540550.1:c.531A>G XP_011538852.1:p.Glu177=
NM_007272.3:c.677A>G MANE Select NP_009203.2:p.Asn226Ser
Search 100 bp 5'
Search 100 bp 3'