Canonical Allele Identifier: CA338567884
Gene: CTRC HGNC NCBI

Linked Data

gnomAD v4: 1-15445700-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445700A>G , CM000663.2:g.15445700A>G GRCh38
NC_000001.10:g.15772195A>G , CM000663.1:g.15772195A>G GRCh37
NC_000001.9:g.15644782A>G NCBI36
NG_009253.1:g.12258A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.743A>G MANE Select ENSP00000365116.4:p.Lys248Arg
ENST00000375943.6:c.*197A>G ENSP00000365110.2:n.*197A>G
ENST00000375949.4:c.743A>G ENSP00000365116.4:p.Lys248Arg
ENST00000483406.1:n.507A>G
NM_007272.2:c.743A>G NP_009203.2:p.Lys248Arg
XM_011540550.1:c.597A>G XP_011538852.1:p.Glu199=
NM_007272.3:c.743A>G MANE Select NP_009203.2:p.Lys248Arg