Canonical Allele Identifier: CA365049659

Gene: RIPPLY2

Linked Data

• MyVariant Identifiers: chr6:g.84566963T>G (hg19) ; chr6:g.83857244T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857244T>G , CM000668.2:g.83857244T>G	GRCh38
NC_000006.11:g.84566963T>G , CM000668.1:g.84566963T>G	GRCh37
NC_000006.10:g.84623682T>G	NCBI36
NG_046722.1:g.8979T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.242T>G MANE Select	ENSP00000358703.1:p.Leu81Arg
ENST00000369687.2:c.68T>G	ENSP00000358701.1:p.Leu23Arg
ENST00000369689.5:c.242T>G	ENSP00000358703.1:p.Leu81Arg
ENST00000635617.1:n.3655T>G
NM_001009994.2:c.242T>G	NP_001009994.1:p.Leu81Arg
NR_103525.1:n.299T>G
NR_103525.2:n.237T>G
NM_001009994.3:c.242T>G MANE Select	NP_001009994.1:p.Leu81Arg
NM_001400774.1:c.-28+3083T>G	NP_001387703.1:n.-28+3083T>G
NM_001400899.1:c.305T>G	NP_001387828.1:p.Leu102Arg
NM_001400900.1:c.*3079T>G	NP_001387829.1:n.*3079T>G
NR_174603.1:n.234+3083T>G
NR_174604.1:n.296+3083T>G
NR_174605.1:n.455+3185T>G
NR_174622.1:n.3317T>G