Canonical Allele Identifier: CA2679552891
Gene: RIPPLY2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857141_83857142del , CM000668.2:g.83857141_83857142del GRCh38
NC_000006.11:g.84566860_84566861del , CM000668.1:g.84566860_84566861del GRCh37
NC_000006.10:g.84623579_84623580del NCBI36
NG_046722.1:g.8876_8877del

Transcript Alleles

HGVS Amino-acid change
ENST00000369689.6:c.240-101_240-100del MANE Select ENSP00000358703.1:n.240-101_240-100del
ENST00000369687.2:c.66-101_66-100del ENSP00000358701.1:n.66-101_66-100del
ENST00000369689.5:c.240-101_240-100del ENSP00000358703.1:n.240-101_240-100del
ENST00000635617.1:n.3552_3553del
NM_001009994.2:c.240-101_240-100del NP_001009994.1:n.240-101_240-100del
NR_103525.1:n.297-101_297-100del
NR_103525.2:n.235-101_235-100del
NM_001009994.3:c.240-101_240-100del MANE Select NP_001009994.1:n.240-101_240-100del
NM_001400774.1:c.-28+2980_-28+2981del NP_001387703.1:n.-28+2980_-28+2981del
NM_001400899.1:c.303-101_303-100del NP_001387828.1:n.303-101_303-100del
NM_001400900.1:c.*2976_*2977del NP_001387829.1:n.*2976_*2977del
NR_174603.1:n.234+2980_234+2981del
NR_174604.1:n.296+2980_296+2981del
NR_174605.1:n.455+3082_455+3083del
NR_174622.1:n.3214_3215del