Canonical Allele Identifier: CA351286382

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241516078A>T (hg19) ; chr2:g.240576661A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576661A>T , CM000664.2:g.240576661A>T	GRCh38
NC_000002.11:g.241516078A>T , CM000664.1:g.241516078A>T	GRCh37
NC_000002.10:g.241164751A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1637A>T MANE Select	ENSP00000270357.4:p.Asp546Val
ENST00000270357.8:c.944A>T	ENSP00000270357.3:p.Asp315Val
ENST00000437406.1:c.203A>T	ENSP00000403319.1:p.Asp68Val
ENST00000451363.5:c.278A>T	ENSP00000414661.1:p.Asp93Val
ENST00000464550.5:n.473A>T
ENST00000471657.1:n.440A>T
ENST00000481757.5:n.2571A>T
ENST00000486058.5:n.1750A>T
ENST00000493398.5:n.783A>T
NM_018226.4:c.1637A>T	NP_060696.4:p.Asp546Val
XM_005247036.3:c.1604A>T	XP_005247093.1:p.Asp535Val
NM_018226.5:c.1637A>T	NP_060696.4:p.Asp546Val
XM_005247036.4:c.1604A>T	XP_005247093.1:p.Asp535Val
NM_018226.6:c.1637A>T MANE Select	NP_060696.4:p.Asp546Val