Canonical Allele Identifier: CA451210581
Gene: RIPPLY2 HGNC NCBI

Linked Data

gnomAD v4: 6-83857296-T-C
MyVariant Identifiers: chr6:g.84567015T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857296T>C , CM000668.2:g.83857296T>C GRCh38
NC_000006.11:g.84567015T>C , CM000668.1:g.84567015T>C GRCh37
NC_000006.10:g.84623734T>C NCBI36
NG_046722.1:g.9031T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369689.6:c.294T>C MANE Select ENSP00000358703.1:p.Ala98=
ENST00000369687.2:c.120T>C ENSP00000358701.1:p.Ala40=
ENST00000369689.5:c.294T>C ENSP00000358703.1:p.Ala98=
ENST00000635617.1:n.3707T>C
NM_001009994.2:c.294T>C NP_001009994.1:p.Ala98=
NR_103525.1:n.351T>C
NR_103525.2:n.289T>C
NM_001009994.3:c.294T>C MANE Select NP_001009994.1:p.Ala98=
NM_001400774.1:c.-28+3135T>C NP_001387703.1:n.-28+3135T>C
NM_001400899.1:c.357T>C NP_001387828.1:p.Ala119=
NM_001400900.1:c.*3131T>C NP_001387829.1:n.*3131T>C
NR_174603.1:n.234+3135T>C
NR_174604.1:n.296+3135T>C
NR_174605.1:n.455+3237T>C
NR_174622.1:n.3369T>C