Canonical Allele Identifier: CA365049716

Gene: RIPPLY2

Linked Data

• MyVariant Identifiers: chr6:g.84566987A>T (hg19) ; chr6:g.83857268A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.83857268A>T , CM000668.2:g.83857268A>T	GRCh38
NC_000006.11:g.84566987A>T , CM000668.1:g.84566987A>T	GRCh37
NC_000006.10:g.84623706A>T	NCBI36
NG_046722.1:g.9003A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.266A>T MANE Select	ENSP00000358703.1:p.Tyr89Phe
ENST00000369687.2:c.92A>T	ENSP00000358701.1:p.Tyr31Phe
ENST00000369689.5:c.266A>T	ENSP00000358703.1:p.Tyr89Phe
ENST00000635617.1:n.3679A>T
NM_001009994.2:c.266A>T	NP_001009994.1:p.Tyr89Phe
NR_103525.1:n.323A>T
NR_103525.2:n.261A>T
NM_001009994.3:c.266A>T MANE Select	NP_001009994.1:p.Tyr89Phe
NM_001400774.1:c.-28+3107A>T	NP_001387703.1:n.-28+3107A>T
NM_001400899.1:c.329A>T	NP_001387828.1:p.Tyr110Phe
NM_001400900.1:c.*3103A>T	NP_001387829.1:n.*3103A>T
NR_174603.1:n.234+3107A>T
NR_174604.1:n.296+3107A>T
NR_174605.1:n.455+3209A>T
NR_174622.1:n.3341A>T