Canonical Allele Identifier: CA365049677

Gene: RIPPLY2

Linked Data

• gnomAD v4: 6-83857252-C-G
• MyVariant Identifiers: chr6:g.84566971C>G (hg19) ; chr6:g.83857252C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857252C>G , CM000668.2:g.83857252C>G	GRCh38
NC_000006.11:g.84566971C>G , CM000668.1:g.84566971C>G	GRCh37
NC_000006.10:g.84623690C>G	NCBI36
NG_046722.1:g.8987C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.250C>G MANE Select	ENSP00000358703.1:p.Pro84Ala
ENST00000369687.2:c.76C>G	ENSP00000358701.1:p.Pro26Ala
ENST00000369689.5:c.250C>G	ENSP00000358703.1:p.Pro84Ala
ENST00000635617.1:n.3663C>G
NM_001009994.2:c.250C>G	NP_001009994.1:p.Pro84Ala
NR_103525.1:n.307C>G
NR_103525.2:n.245C>G
NM_001009994.3:c.250C>G MANE Select	NP_001009994.1:p.Pro84Ala
NM_001400774.1:c.-28+3091C>G	NP_001387703.1:n.-28+3091C>G
NM_001400899.1:c.313C>G	NP_001387828.1:p.Pro105Ala
NM_001400900.1:c.*3087C>G	NP_001387829.1:n.*3087C>G
NR_174603.1:n.234+3091C>G
NR_174604.1:n.296+3091C>G
NR_174605.1:n.455+3193C>G
NR_174622.1:n.3325C>G