Canonical Allele Identifier: CA1091253044
Gene: RIPPLY2 HGNC NCBI

Linked Data

dbSNP Id: rs2099455112
gnomAD v3: 6-83857174-T-C
gnomAD v4: 6-83857174-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857174T>C , CM000668.2:g.83857174T>C GRCh38
NC_000006.11:g.84566893T>C , CM000668.1:g.84566893T>C GRCh37
NC_000006.10:g.84623612T>C NCBI36
NG_046722.1:g.8909T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369689.6:c.240-68T>C MANE Select ENSP00000358703.1:n.240-68T>C
ENST00000369687.2:c.66-68T>C ENSP00000358701.1:n.66-68T>C
ENST00000369689.5:c.240-68T>C ENSP00000358703.1:n.240-68T>C
ENST00000635617.1:n.3585T>C
NM_001009994.2:c.240-68T>C NP_001009994.1:n.240-68T>C
NR_103525.1:n.297-68T>C
NR_103525.2:n.235-68T>C
NM_001009994.3:c.240-68T>C MANE Select NP_001009994.1:n.240-68T>C
NM_001400774.1:c.-28+3013T>C NP_001387703.1:n.-28+3013T>C
NM_001400899.1:c.303-68T>C NP_001387828.1:n.303-68T>C
NM_001400900.1:c.*3009T>C NP_001387829.1:n.*3009T>C
NR_174603.1:n.234+3013T>C
NR_174604.1:n.296+3013T>C
NR_174605.1:n.455+3115T>C
NR_174622.1:n.3247T>C