Canonical Allele Identifier: CA451210568
Gene: RIPPLY2 HGNC NCBI

Linked Data

gnomAD v4: 6-83857263-A-G
MyVariant Identifiers: chr6:g.84566982A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.83857263A>G , CM000668.2:g.83857263A>G GRCh38
NC_000006.11:g.84566982A>G , CM000668.1:g.84566982A>G GRCh37
NC_000006.10:g.84623701A>G NCBI36
NG_046722.1:g.8998A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369689.6:c.261A>G MANE Select ENSP00000358703.1:p.Lys87=
ENST00000369687.2:c.87A>G ENSP00000358701.1:p.Lys29=
ENST00000369689.5:c.261A>G ENSP00000358703.1:p.Lys87=
ENST00000635617.1:n.3674A>G
NM_001009994.2:c.261A>G NP_001009994.1:p.Lys87=
NR_103525.1:n.318A>G
NR_103525.2:n.256A>G
NM_001009994.3:c.261A>G MANE Select NP_001009994.1:p.Lys87=
NM_001400774.1:c.-28+3102A>G NP_001387703.1:n.-28+3102A>G
NM_001400899.1:c.324A>G NP_001387828.1:p.Lys108=
NM_001400900.1:c.*3098A>G NP_001387829.1:n.*3098A>G
NR_174603.1:n.234+3102A>G
NR_174604.1:n.296+3102A>G
NR_174605.1:n.455+3204A>G
NR_174622.1:n.3336A>G