Canonical Allele Identifier: CA451210579
Gene: RIPPLY2 HGNC NCBI

Linked Data

gnomAD v4: 6-83857293-A-G
MyVariant Identifiers: chr6:g.84567012A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857293A>G , CM000668.2:g.83857293A>G GRCh38
NC_000006.11:g.84567012A>G , CM000668.1:g.84567012A>G GRCh37
NC_000006.10:g.84623731A>G NCBI36
NG_046722.1:g.9028A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369689.6:c.291A>G MANE Select ENSP00000358703.1:p.Glu97=
ENST00000369687.2:c.117A>G ENSP00000358701.1:p.Glu39=
ENST00000369689.5:c.291A>G ENSP00000358703.1:p.Glu97=
ENST00000635617.1:n.3704A>G
NM_001009994.2:c.291A>G NP_001009994.1:p.Glu97=
NR_103525.1:n.348A>G
NR_103525.2:n.286A>G
NM_001009994.3:c.291A>G MANE Select NP_001009994.1:p.Glu97=
NM_001400774.1:c.-28+3132A>G NP_001387703.1:n.-28+3132A>G
NM_001400899.1:c.354A>G NP_001387828.1:p.Glu118=
NM_001400900.1:c.*3128A>G NP_001387829.1:n.*3128A>G
NR_174603.1:n.234+3132A>G
NR_174604.1:n.296+3132A>G
NR_174605.1:n.455+3234A>G
NR_174622.1:n.3366A>G