Canonical Allele Identifier: CA365049649

Gene: RIPPLY2

Linked Data

• COSMIC: COSM1082117
• MyVariant Identifiers: chr6:g.84566959A>G (hg19) ; chr6:g.83857240A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857240A>G , CM000668.2:g.83857240A>G	GRCh38
NC_000006.11:g.84566959A>G , CM000668.1:g.84566959A>G	GRCh37
NC_000006.10:g.84623678A>G	NCBI36
NG_046722.1:g.8975A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.240-2A>G MANE Select	ENSP00000358703.1:n.240-2A>G
ENST00000369687.2:c.66-2A>G	ENSP00000358701.1:n.66-2A>G
ENST00000369689.5:c.240-2A>G	ENSP00000358703.1:n.240-2A>G
ENST00000635617.1:n.3651A>G
NM_001009994.2:c.240-2A>G	NP_001009994.1:n.240-2A>G
NR_103525.1:n.297-2A>G
NR_103525.2:n.235-2A>G
NM_001009994.3:c.240-2A>G MANE Select	NP_001009994.1:n.240-2A>G
NM_001400774.1:c.-28+3079A>G	NP_001387703.1:n.-28+3079A>G
NM_001400899.1:c.303-2A>G	NP_001387828.1:n.303-2A>G
NM_001400900.1:c.*3075A>G	NP_001387829.1:n.*3075A>G
NR_174603.1:n.234+3079A>G
NR_174604.1:n.296+3079A>G
NR_174605.1:n.455+3181A>G
NR_174622.1:n.3313A>G