Canonical Allele Identifier: CA451210565

Gene: RIPPLY2

Linked Data

• MyVariant Identifiers: chr6:g.84566979A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857260A>C , CM000668.2:g.83857260A>C	GRCh38
NC_000006.11:g.84566979A>C , CM000668.1:g.84566979A>C	GRCh37
NC_000006.10:g.84623698A>C	NCBI36
NG_046722.1:g.8995A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.258A>C MANE Select	ENSP00000358703.1:p.Ser86=
ENST00000369687.2:c.84A>C	ENSP00000358701.1:p.Ser28=
ENST00000369689.5:c.258A>C	ENSP00000358703.1:p.Ser86=
ENST00000635617.1:n.3671A>C
NM_001009994.2:c.258A>C	NP_001009994.1:p.Ser86=
NR_103525.1:n.315A>C
NR_103525.2:n.253A>C
NM_001009994.3:c.258A>C MANE Select	NP_001009994.1:p.Ser86=
NM_001400774.1:c.-28+3099A>C	NP_001387703.1:n.-28+3099A>C
NM_001400899.1:c.321A>C	NP_001387828.1:p.Ser107=
NM_001400900.1:c.*3095A>C	NP_001387829.1:n.*3095A>C
NR_174603.1:n.234+3099A>C
NR_174604.1:n.296+3099A>C
NR_174605.1:n.455+3201A>C
NR_174622.1:n.3333A>C