Canonical Allele Identifier: CA338567859
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445687A>T , CM000663.2:g.15445687A>T GRCh38
NC_000001.10:g.15772182A>T , CM000663.1:g.15772182A>T GRCh37
NC_000001.9:g.15644769A>T NCBI36
NG_009253.1:g.12245A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.730A>T MANE Select ENSP00000365116.4:p.Asn244Tyr
ENST00000375943.6:c.*184A>T ENSP00000365110.2:n.*184A>T
ENST00000375949.4:c.730A>T ENSP00000365116.4:p.Asn244Tyr
ENST00000483406.1:n.494A>T
NM_007272.2:c.730A>T NP_009203.2:p.Asn244Tyr
XM_011540550.1:c.584A>T XP_011538852.1:p.Gln195Leu
NM_007272.3:c.730A>T MANE Select NP_009203.2:p.Asn244Tyr