Canonical Allele Identifier: CA2984463963
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132419863_132419864insA , CM000667.2:g.132419863_132419864insA GRCh38
NC_000005.9:g.131755555_131755556insA , CM000667.1:g.131755555_131755556insA GRCh37
NC_000005.8:g.131783454_131783455insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000638452.2:c.-286_-285insA ENSP00000492349.2:n.-286_-285insA
ENST00000638504.1:n.129_130insA
ENST00000638568.2:c.-428_-427insA ENSP00000491158.2:n.-428_-427insA
ENST00000639899.1:n.172_173insA
ENST00000337752.6:c.-30_-29insA (CARINH) ENSP00000338228.2:n.-30_-29insA
ENST00000378947.7:c.-30_-29insA (CARINH) ENSP00000368230.3:n.-30_-29insA
ENST00000378953.8:c.-30_-29insA (CARINH) ENSP00000368236.4:n.-30_-29insA
ENST00000407797.5:c.-30_-29insA (CARINH) ENSP00000385513.1:n.-30_-29insA
ENST00000461203.5:n.102_103insA (CARINH)
ENST00000621237.1:c.-29-1_-29insA (CARINH) ENSP00000481774.1:n.-29-1_-29insA
NR_045116.1:n.310_311insA (CARINH)
NM_001207001.2:c.-30_-29insA (CARINH) NP_001193930.1:n.-30_-29insA
XR_948788.3:n.894-115_894-114insT (LINC02863)
NR_161242.1:n.154_155insA (CARINH)