Canonical Allele Identifier: CA365049702

Gene: RIPPLY2

Linked Data

• MyVariant Identifiers: chr6:g.84566982A>C (hg19) ; chr6:g.83857263A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369689.6:c.261A>C MANE Select	ENSP00000358703.1:p.Lys87Asn
ENST00000369687.2:c.87A>C	ENSP00000358701.1:p.Lys29Asn
ENST00000369689.5:c.261A>C	ENSP00000358703.1:p.Lys87Asn
ENST00000635617.1:n.3674A>C
NM_001009994.2:c.261A>C	NP_001009994.1:p.Lys87Asn
NR_103525.1:n.318A>C
NR_103525.2:n.256A>C
NM_001009994.3:c.261A>C MANE Select	NP_001009994.1:p.Lys87Asn
NM_001400774.1:c.-28+3102A>C	NP_001387703.1:n.-28+3102A>C
NM_001400899.1:c.324A>C	NP_001387828.1:p.Lys108Asn
NM_001400900.1:c.*3098A>C	NP_001387829.1:n.*3098A>C
NR_174603.1:n.234+3102A>C
NR_174604.1:n.296+3102A>C
NR_174605.1:n.455+3204A>C
NR_174622.1:n.3336A>C