Canonical Allele Identifier: CA142674786
Gene: RIPPLY2 HGNC NCBI

Linked Data

dbSNP Id: rs985959923
gnomAD v2: 6-84566864-C-T
gnomAD v3: 6-83857145-C-T
gnomAD v4: 6-83857145-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857145C>T , CM000668.2:g.83857145C>T GRCh38
NC_000006.11:g.84566864C>T , CM000668.1:g.84566864C>T GRCh37
NC_000006.10:g.84623583C>T NCBI36
NG_046722.1:g.8880C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369689.6:c.240-97C>T MANE Select ENSP00000358703.1:n.240-97C>T
ENST00000369687.2:c.66-97C>T ENSP00000358701.1:n.66-97C>T
ENST00000369689.5:c.240-97C>T ENSP00000358703.1:n.240-97C>T
ENST00000635617.1:n.3556C>T
NM_001009994.2:c.240-97C>T NP_001009994.1:n.240-97C>T
NR_103525.1:n.297-97C>T
NR_103525.2:n.235-97C>T
NM_001009994.3:c.240-97C>T MANE Select NP_001009994.1:n.240-97C>T
NM_001400774.1:c.-28+2984C>T NP_001387703.1:n.-28+2984C>T
NM_001400899.1:c.303-97C>T NP_001387828.1:n.303-97C>T
NM_001400900.1:c.*2980C>T NP_001387829.1:n.*2980C>T
NR_174603.1:n.234+2984C>T
NR_174604.1:n.296+2984C>T
NR_174605.1:n.455+3086C>T
NR_174622.1:n.3218C>T