Canonical Allele Identifier: CA365049699
Gene: RIPPLY2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857262A>C , CM000668.2:g.83857262A>C GRCh38
NC_000006.11:g.84566981A>C , CM000668.1:g.84566981A>C GRCh37
NC_000006.10:g.84623700A>C NCBI36
NG_046722.1:g.8997A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369689.6:c.260A>C MANE Select ENSP00000358703.1:p.Lys87Thr
ENST00000369687.2:c.86A>C ENSP00000358701.1:p.Lys29Thr
ENST00000369689.5:c.260A>C ENSP00000358703.1:p.Lys87Thr
ENST00000635617.1:n.3673A>C
NM_001009994.2:c.260A>C NP_001009994.1:p.Lys87Thr
NR_103525.1:n.317A>C
NR_103525.2:n.255A>C
NM_001009994.3:c.260A>C MANE Select NP_001009994.1:p.Lys87Thr
NM_001400774.1:c.-28+3101A>C NP_001387703.1:n.-28+3101A>C
NM_001400899.1:c.323A>C NP_001387828.1:p.Lys108Thr
NM_001400900.1:c.*3097A>C NP_001387829.1:n.*3097A>C
NR_174603.1:n.234+3101A>C
NR_174604.1:n.296+3101A>C
NR_174605.1:n.455+3203A>C
NR_174622.1:n.3335A>C