Canonical Allele Identifier: CA2600616191

Gene: RIPPLY2

Linked Data

• dbSNP Id: rs2129125793
• gnomAD v3: 6-83857193-T-A
• gnomAD v4: 6-83857193-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857193T>A , CM000668.2:g.83857193T>A	GRCh38
NC_000006.11:g.84566912T>A , CM000668.1:g.84566912T>A	GRCh37
NC_000006.10:g.84623631T>A	NCBI36
NG_046722.1:g.8928T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.240-49T>A MANE Select	ENSP00000358703.1:n.240-49T>A
ENST00000369687.2:c.66-49T>A	ENSP00000358701.1:n.66-49T>A
ENST00000369689.5:c.240-49T>A	ENSP00000358703.1:n.240-49T>A
ENST00000635617.1:n.3604T>A
NM_001009994.2:c.240-49T>A	NP_001009994.1:n.240-49T>A
NR_103525.1:n.297-49T>A
NR_103525.2:n.235-49T>A
NM_001009994.3:c.240-49T>A MANE Select	NP_001009994.1:n.240-49T>A
NM_001400774.1:c.-28+3032T>A	NP_001387703.1:n.-28+3032T>A
NM_001400899.1:c.303-49T>A	NP_001387828.1:n.303-49T>A
NM_001400900.1:c.*3028T>A	NP_001387829.1:n.*3028T>A
NR_174603.1:n.234+3032T>A
NR_174604.1:n.296+3032T>A
NR_174605.1:n.455+3134T>A
NR_174622.1:n.3266T>A