Canonical Allele Identifier: CA2675201580
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419847_132419848del , CM000667.2:g.132419847_132419848del GRCh38
NC_000005.9:g.131755539_131755540del , CM000667.1:g.131755539_131755540del GRCh37
NC_000005.8:g.131783438_131783439del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-302_-301del ENSP00000492349.2:n.-302_-301del
ENST00000638504.1:n.113_114del
ENST00000638568.2:c.-444_-443del ENSP00000491158.2:n.-444_-443del
ENST00000639899.1:n.156_157del
ENST00000337752.6:c.-46_-45del (CARINH) ENSP00000338228.2:n.-46_-45del
ENST00000378947.7:c.-46_-45del (CARINH) ENSP00000368230.3:n.-46_-45del
ENST00000378953.8:c.-46_-45del (CARINH) ENSP00000368236.4:n.-46_-45del
ENST00000407797.5:c.-46_-45del (CARINH) ENSP00000385513.1:n.-46_-45del
ENST00000461203.5:n.86_87del (CARINH)
NR_045116.1:n.294_295del (CARINH)
NM_001207001.2:c.-46_-45del (CARINH) NP_001193930.1:n.-46_-45del
XR_948788.3:n.894-98_894-97del (LINC02863)
NR_161242.1:n.138_139del (CARINH)