Canonical Allele Identifier: CA142674790

Gene: RIPPLY2

Linked Data

• dbSNP Id: rs199862676
• gnomAD v3: 6-83857283-A-C
• gnomAD v4: 6-83857283-A-C
• MyVariant Identifiers: chr6:g.84567002A>C (hg19) ; chr6:g.83857283A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857283A>C , CM000668.2:g.83857283A>C	GRCh38
NC_000006.11:g.84567002A>C , CM000668.1:g.84567002A>C	GRCh37
NC_000006.10:g.84623721A>C	NCBI36
NG_046722.1:g.9018A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.281A>C MANE Select	ENSP00000358703.1:p.Gln94Pro
ENST00000369687.2:c.107A>C	ENSP00000358701.1:p.Gln36Pro
ENST00000369689.5:c.281A>C	ENSP00000358703.1:p.Gln94Pro
ENST00000635617.1:n.3694A>C
NM_001009994.2:c.281A>C	NP_001009994.1:p.Gln94Pro
NR_103525.1:n.338A>C
NR_103525.2:n.276A>C
NM_001009994.3:c.281A>C MANE Select	NP_001009994.1:p.Gln94Pro
NM_001400774.1:c.-28+3122A>C	NP_001387703.1:n.-28+3122A>C
NM_001400899.1:c.344A>C	NP_001387828.1:p.Gln115Pro
NM_001400900.1:c.*3118A>C	NP_001387829.1:n.*3118A>C
NR_174603.1:n.234+3122A>C
NR_174604.1:n.296+3122A>C
NR_174605.1:n.455+3224A>C
NR_174622.1:n.3356A>C