Canonical Allele Identifier: CA562780214

Gene: CARINH LINC02863

Linked Data

• dbSNP Id: rs1561584538
• gnomAD v2: 5-131755751-GGTTT-G
• gnomAD v3: 5-132420059-GGTTT-G
• gnomAD v4: 5-132420059-GGTTT-G
• MyVariant Identifiers: chr5:g.131755752_131755755del (hg19) ; chr5:g.132420060_132420063del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132420060_132420063del , CM000667.2:g.132420060_132420063del	GRCh38
NC_000005.9:g.131755752_131755755del , CM000667.1:g.131755752_131755755del	GRCh37
NC_000005.8:g.131783651_131783654del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638452.2:c.-209+120_-209+123del	ENSP00000492349.2:n.-209+120_-209+123del
ENST00000638504.1:n.206+120_206+123del
ENST00000638568.2:c.-351+120_-351+123del	ENSP00000491158.2:n.-351+120_-351+123del
ENST00000639899.1:n.249+120_249+123del
ENST00000337752.6:c.48+120_48+123del (CARINH)	ENSP00000338228.2:n.48+120_48+123del
ENST00000378947.7:c.48+120_48+123del (CARINH)	ENSP00000368230.3:n.48+120_48+123del
ENST00000378953.8:c.48+120_48+123del (CARINH)	ENSP00000368236.4:n.48+120_48+123del
ENST00000407797.5:c.48+120_48+123del (CARINH)	ENSP00000385513.1:n.48+120_48+123del
ENST00000461203.5:n.179+120_179+123del (CARINH)
ENST00000621237.1:c.48+120_48+123del (CARINH)	ENSP00000481774.1:n.48+120_48+123del
NR_045116.1:n.387+120_387+123del (CARINH)
NM_001207001.2:c.48+120_48+123del (CARINH)	NP_001193930.1:n.48+120_48+123del
XR_948788.3:n.894-314_894-311del (LINC02863)
NR_161242.1:n.231+120_231+123del (CARINH)