Canonical Allele Identifier: CA451210558
Gene: RIPPLY2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.84566964A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857245A>G , CM000668.2:g.83857245A>G GRCh38
NC_000006.11:g.84566964A>G , CM000668.1:g.84566964A>G GRCh37
NC_000006.10:g.84623683A>G NCBI36
NG_046722.1:g.8980A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369689.6:c.243A>G MANE Select ENSP00000358703.1:p.Leu81=
ENST00000369687.2:c.69A>G ENSP00000358701.1:p.Leu23=
ENST00000369689.5:c.243A>G ENSP00000358703.1:p.Leu81=
ENST00000635617.1:n.3656A>G
NM_001009994.2:c.243A>G NP_001009994.1:p.Leu81=
NR_103525.1:n.300A>G
NR_103525.2:n.238A>G
NM_001009994.3:c.243A>G MANE Select NP_001009994.1:p.Leu81=
NM_001400774.1:c.-28+3084A>G NP_001387703.1:n.-28+3084A>G
NM_001400899.1:c.306A>G NP_001387828.1:p.Leu102=
NM_001400900.1:c.*3080A>G NP_001387829.1:n.*3080A>G
NR_174603.1:n.234+3084A>G
NR_174604.1:n.296+3084A>G
NR_174605.1:n.455+3186A>G
NR_174622.1:n.3318A>G