Canonical Allele Identifier: CA12203305
Community Standard Title: NM_018292.5(QRSL1):c.-55G>A
Gene: QRSL1 HGNC NCBI
RTN4IP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.106629627G>A , CM000668.2:g.106629627G>A GRCh38
NC_000006.11:g.107077502G>A , CM000668.1:g.107077502G>A GRCh37
NC_000006.10:g.107184195G>A NCBI36
NG_047205.1:g.5874C>T

Transcript Alleles

HGVS Amino-acid Change
NM_018292.5:c.-55G>A (QRSL1) MANE Select NP_060762.3:n.-55G>A
ENST00000369046.8:c.-55G>A (QRSL1) MANE Select ENSP00000358042.4:n.-55G>A
NM_001318746.1:c.-27+700C>T (RTN4IP1) NP_001305675.1:n.-27+700C>T
NM_018292.4:c.-55G>A (QRSL1) NP_060762.3:n.-55G>A
ENST00000369044.1:c.-55G>A (QRSL1) ENSP00000358040.1:n.-55G>A
ENST00000467262.1:n.29G>A (QRSL1)
XM_011535924.1:c.-434G>A (QRSL1) XP_011534226.1:n.-434G>A
XM_011535924.2:c.-434G>A (QRSL1) XP_011534226.1:n.-434G>A
XM_011536192.1:c.34+216C>T (RTN4IP1) XP_011534494.1:n.34+216C>T
XM_011536192.2:c.34+216C>T (RTN4IP1) XP_011534494.1:n.34+216C>T
XM_011536193.1:c.-27+700C>T (RTN4IP1) XP_011534495.1:n.-27+700C>T
XR_001743693.2:n.691C>T (RTN4IP1)