Canonical Allele Identifier: CA365049684

Gene: RIPPLY2

Linked Data

• MyVariant Identifiers: chr6:g.84566974A>C (hg19) ; chr6:g.83857255A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857255A>C , CM000668.2:g.83857255A>C	GRCh38
NC_000006.11:g.84566974A>C , CM000668.1:g.84566974A>C	GRCh37
NC_000006.10:g.84623693A>C	NCBI36
NG_046722.1:g.8990A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.253A>C MANE Select	ENSP00000358703.1:p.Lys85Gln
ENST00000369687.2:c.79A>C	ENSP00000358701.1:p.Lys27Gln
ENST00000369689.5:c.253A>C	ENSP00000358703.1:p.Lys85Gln
ENST00000635617.1:n.3666A>C
NM_001009994.2:c.253A>C	NP_001009994.1:p.Lys85Gln
NR_103525.1:n.310A>C
NR_103525.2:n.248A>C
NM_001009994.3:c.253A>C MANE Select	NP_001009994.1:p.Lys85Gln
NM_001400774.1:c.-28+3094A>C	NP_001387703.1:n.-28+3094A>C
NM_001400899.1:c.316A>C	NP_001387828.1:p.Lys106Gln
NM_001400900.1:c.*3090A>C	NP_001387829.1:n.*3090A>C
NR_174603.1:n.234+3094A>C
NR_174604.1:n.296+3094A>C
NR_174605.1:n.455+3196A>C
NR_174622.1:n.3328A>C