Canonical Allele Identifier: CA2742588026
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445953_15445972dup , CM000663.2:g.15445953_15445972dup GRCh38
NC_000001.10:g.15772448_15772467dup , CM000663.1:g.15772448_15772467dup GRCh37
NC_000001.9:g.15645035_15645054dup NCBI36
NG_009253.1:g.12511_12530dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+204_792+223dup MANE Select ENSP00000365116.4:n.792+204_792+223dup
ENST00000375943.6:c.*246+204_*246+223dup ENSP00000365110.2:n.*246+204_*246+223dup
ENST00000375949.4:c.792+204_792+223dup ENSP00000365116.4:n.792+204_792+223dup
ENST00000483406.1:n.556+204_556+223dup
NM_007272.2:c.792+204_792+223dup NP_009203.2:n.792+204_792+223dup
XM_011540550.1:c.646+204_646+223dup XP_011538852.1:n.646+204_646+223dup
NM_007272.3:c.792+204_792+223dup MANE Select NP_009203.2:n.792+204_792+223dup