Canonical Allele Identifier: CA1583158556
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419781_132419782delinsAT , CM000667.2:g.132419781_132419782delinsAT GRCh38
NC_000005.9:g.131755473_131755474delinsAT , CM000667.1:g.131755473_131755474delinsAT GRCh37
NC_000005.8:g.131783372_131783373delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-326-42_-326-41delinsAT ENSP00000492349.2:n.-326-42_-326-41delinsAT
ENST00000638504.1:n.89-42_89-41delinsAT
ENST00000638568.2:c.-468-42_-468-41delinsAT ENSP00000491158.2:n.-468-42_-468-41delinsAT
ENST00000639899.1:n.132-42_132-41delinsAT
ENST00000337752.6:c.-70-42_-70-41delinsAT (CARINH) ENSP00000338228.2:n.-70-42_-70-41delinsAT
ENST00000378947.7:c.-70-42_-70-41delinsAT (CARINH) ENSP00000368230.3:n.-70-42_-70-41delinsAT
ENST00000378953.8:c.-70-42_-70-41delinsAT (CARINH) ENSP00000368236.4:n.-70-42_-70-41delinsAT
ENST00000407797.5:c.-70-42_-70-41delinsAT (CARINH) ENSP00000385513.1:n.-70-42_-70-41delinsAT
ENST00000461203.5:n.62-42_62-41delinsAT (CARINH)
NR_045116.1:n.270-42_270-41delinsAT (CARINH)
NM_001207001.2:c.-70-42_-70-41delinsAT (CARINH) NP_001193930.1:n.-70-42_-70-41delinsAT
XR_948788.3:n.894-33_894-32delinsAT (LINC02863)
NR_161242.1:n.114-42_114-41delinsAT (CARINH)