Canonical Allele Identifier: CA451210572
Gene: RIPPLY2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.84566991T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857272T>C , CM000668.2:g.83857272T>C GRCh38
NC_000006.11:g.84566991T>C , CM000668.1:g.84566991T>C GRCh37
NC_000006.10:g.84623710T>C NCBI36
NG_046722.1:g.9007T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369689.6:c.270T>C MANE Select ENSP00000358703.1:p.Asp90=
ENST00000369687.2:c.96T>C ENSP00000358701.1:p.Asp32=
ENST00000369689.5:c.270T>C ENSP00000358703.1:p.Asp90=
ENST00000635617.1:n.3683T>C
NM_001009994.2:c.270T>C NP_001009994.1:p.Asp90=
NR_103525.1:n.327T>C
NR_103525.2:n.265T>C
NM_001009994.3:c.270T>C MANE Select NP_001009994.1:p.Asp90=
NM_001400774.1:c.-28+3111T>C NP_001387703.1:n.-28+3111T>C
NM_001400899.1:c.333T>C NP_001387828.1:p.Asp111=
NM_001400900.1:c.*3107T>C NP_001387829.1:n.*3107T>C
NR_174603.1:n.234+3111T>C
NR_174604.1:n.296+3111T>C
NR_174605.1:n.455+3213T>C
NR_174622.1:n.3345T>C