Canonical Allele Identifier: CA2679552915
Gene: RIPPLY2 HGNC NCBI

Linked Data

gnomAD v4: 6-83857183-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857183T>C , CM000668.2:g.83857183T>C GRCh38
NC_000006.11:g.84566902T>C , CM000668.1:g.84566902T>C GRCh37
NC_000006.10:g.84623621T>C NCBI36
NG_046722.1:g.8918T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369689.6:c.240-59T>C MANE Select ENSP00000358703.1:n.240-59T>C
ENST00000369687.2:c.66-59T>C ENSP00000358701.1:n.66-59T>C
ENST00000369689.5:c.240-59T>C ENSP00000358703.1:n.240-59T>C
ENST00000635617.1:n.3594T>C
NM_001009994.2:c.240-59T>C NP_001009994.1:n.240-59T>C
NR_103525.1:n.297-59T>C
NR_103525.2:n.235-59T>C
NM_001009994.3:c.240-59T>C MANE Select NP_001009994.1:n.240-59T>C
NM_001400774.1:c.-28+3022T>C NP_001387703.1:n.-28+3022T>C
NM_001400899.1:c.303-59T>C NP_001387828.1:n.303-59T>C
NM_001400900.1:c.*3018T>C NP_001387829.1:n.*3018T>C
NR_174603.1:n.234+3022T>C
NR_174604.1:n.296+3022T>C
NR_174605.1:n.455+3124T>C
NR_174622.1:n.3256T>C