Canonical Allele Identifier: CA90987146
Community Standard Title: NM_000996.4(RPL35A):c.278C>T (p.Pro93Leu)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.197954116C>T , CM000665.2:g.197954116C>T GRCh38
NC_000003.11:g.197680987C>T , CM000665.1:g.197680987C>T GRCh37
NC_000003.10:g.199165384C>T NCBI36
NG_011743.1:g.8936C>T
NG_033072.1:g.10900G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000996.4:c.278C>T (RPL35A) MANE Select NP_000987.2:p.Pro93Leu
NM_032263.5:c.-60+5413G>A (IQCG) MANE Select NP_115639.1:n.-60+5413G>A
ENST00000265239.11:c.-60+5413G>A (IQCG) MANE Select ENSP00000265239.6:n.-60+5413G>A
ENST00000647248.2:c.278C>T (RPL35A) MANE Select ENSP00000495672.1:p.Pro93Leu
NM_000996.2:c.278C>T (RPL35A) NP_000987.2:p.Pro93Leu
NM_001316311.1:c.278C>T (RPL35A) NP_001303240.1:p.Pro93Leu
NM_001316311.2:c.278C>T (RPL35A) NP_001303240.1:p.Pro93Leu
NM_001323028.1:c.-50+5413G>A (IQCG) NP_001309957.1:n.-50+5413G>A
NM_001323028.2:c.-50+5413G>A (IQCG) NP_001309957.1:n.-50+5413G>A
NM_001323029.1:c.-375+5413G>A (IQCG) NP_001309958.1:n.-375+5413G>A
NM_001323029.2:c.-375+5413G>A (IQCG) NP_001309958.1:n.-375+5413G>A
NM_032263.3:c.-60+5413G>A (IQCG) NP_115639.1:n.-60+5413G>A
NM_032263.4:c.-60+5413G>A (IQCG) NP_115639.1:n.-60+5413G>A
ENST00000265239.10:c.-60+5413G>A (IQCG) ENSP00000265239.6:n.-60+5413G>A
ENST00000329092.12:n.425C>T (RPL35A)
ENST00000416896.1:c.-50+5413G>A (IQCG) ENSP00000406411.1:n.-50+5413G>A
ENST00000429437.5:c.*127C>T (RPL35A) ENSP00000398058.1:n.*127C>T
ENST00000439255.1:c.*277C>T (RPL35A) ENSP00000410683.1:n.*277C>T
ENST00000442341.5:c.278C>T (RPL35A) ENSP00000387688.1:p.Pro93Leu
ENST00000448864.5:c.278C>T (RPL35A) ENSP00000393393.1:p.Pro93Leu
ENST00000448864.6:c.278C>T (RPL35A) ENSP00000393393.1:p.Pro93Leu
ENST00000464167.5:c.278C>T (RPL35A) ENSP00000419117.1:p.Pro93Leu
ENST00000474640.1:n.554C>T (RPL35A)
ENST00000480302.5:n.312+5413G>A (IQCG)
ENST00000485439.5:n.342C>T (RPL35A)
ENST00000642387.1:n.469C>T (RPL35A)
XM_024453790.1:c.-60+5413G>A (IQCG) XP_024309558.1:n.-60+5413G>A
XR_002959600.1:n.356+5413G>A (IQCG)
XR_924190.1:n.356+5413G>A (IQCG)