Canonical Allele Identifier: CA3908900

Gene: RIPPLY2

Linked Data

• dbSNP Id: rs778439554
• ExAC: 6:84566969 G / C
• gnomAD v2: 6-84566969-G-C
• gnomAD v4: 6-83857250-G-C
• MyVariant Identifiers: chr6:g.84566969G>C (hg19) ; chr6:g.83857250G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857250G>C , CM000668.2:g.83857250G>C	GRCh38
NC_000006.11:g.84566969G>C , CM000668.1:g.84566969G>C	GRCh37
NC_000006.10:g.84623688G>C	NCBI36
NG_046722.1:g.8985G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.248G>C MANE Select	ENSP00000358703.1:p.Trp83Ser
ENST00000369687.2:c.74G>C	ENSP00000358701.1:p.Trp25Ser
ENST00000369689.5:c.248G>C	ENSP00000358703.1:p.Trp83Ser
ENST00000635617.1:n.3661G>C
NM_001009994.2:c.248G>C	NP_001009994.1:p.Trp83Ser
NR_103525.1:n.305G>C
NR_103525.2:n.243G>C
NM_001009994.3:c.248G>C MANE Select	NP_001009994.1:p.Trp83Ser
NM_001400774.1:c.-28+3089G>C	NP_001387703.1:n.-28+3089G>C
NM_001400899.1:c.311G>C	NP_001387828.1:p.Trp104Ser
NM_001400900.1:c.*3085G>C	NP_001387829.1:n.*3085G>C
NR_174603.1:n.234+3089G>C
NR_174604.1:n.296+3089G>C
NR_174605.1:n.455+3191G>C
NR_174622.1:n.3323G>C