Canonical Allele Identifier: CA2663966925

Gene: RNPEPL1

Linked Data

• gnomAD v4: 2-240576012-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576012G>T , CM000664.2:g.240576012G>T	GRCh38
NC_000002.11:g.241515429G>T , CM000664.1:g.241515429G>T	GRCh37
NC_000002.10:g.241164102G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000270357.10:c.1510+402G>T MANE Select	ENSP00000270357.4:n.1510+402G>T
ENST00000270357.8:c.817+402G>T	ENSP00000270357.3:n.817+402G>T
ENST00000437406.1:c.109+402G>T	ENSP00000403319.1:n.109+402G>T
ENST00000451363.5:c.151+402G>T	ENSP00000414661.1:n.151+402G>T
ENST00000464550.5:n.346+402G>T
ENST00000471657.1:n.313+402G>T
ENST00000481757.5:n.1922G>T
ENST00000486058.5:n.1623+402G>T
ENST00000493398.5:n.656+402G>T
NM_018226.4:c.1510+402G>T	NP_060696.4:n.1510+402G>T
XM_005247036.3:c.1510+402G>T	XP_005247093.1:n.1510+402G>T
NM_018226.5:c.1510+402G>T	NP_060696.4:n.1510+402G>T
XM_005247036.4:c.1510+402G>T	XP_005247093.1:n.1510+402G>T
NM_018226.6:c.1510+402G>T MANE Select	NP_060696.4:n.1510+402G>T