Canonical Allele Identifier: CA1583158676
Gene: CARINH HGNC NCBI
LINC02863 HGNC NCBI

Linked Data

dbSNP Id: rs1753239839
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132420022_132420031del , CM000667.2:g.132420022_132420031del GRCh38
NC_000005.9:g.131755714_131755723del , CM000667.1:g.131755714_131755723del GRCh37
NC_000005.8:g.131783613_131783622del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638452.2:c.-209+82_-209+91del ENSP00000492349.2:n.-209+82_-209+91del
ENST00000638504.1:n.206+82_206+91del
ENST00000638568.2:c.-351+82_-351+91del ENSP00000491158.2:n.-351+82_-351+91del
ENST00000639899.1:n.249+82_249+91del
ENST00000337752.6:c.48+82_48+91del (CARINH) ENSP00000338228.2:n.48+82_48+91del
ENST00000378947.7:c.48+82_48+91del (CARINH) ENSP00000368230.3:n.48+82_48+91del
ENST00000378953.8:c.48+82_48+91del (CARINH) ENSP00000368236.4:n.48+82_48+91del
ENST00000407797.5:c.48+82_48+91del (CARINH) ENSP00000385513.1:n.48+82_48+91del
ENST00000461203.5:n.179+82_179+91del (CARINH)
ENST00000621237.1:c.48+82_48+91del (CARINH) ENSP00000481774.1:n.48+82_48+91del
NR_045116.1:n.387+82_387+91del (CARINH)
NM_001207001.2:c.48+82_48+91del (CARINH) NP_001193930.1:n.48+82_48+91del
XR_948788.3:n.894-279_894-270del (LINC02863)
NR_161242.1:n.231+82_231+91del (CARINH)
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