Canonical Allele Identifier: CA437855467

Gene: IQCG RPL35A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.197954024C>T , CM000665.2:g.197954024C>T	GRCh38
NC_000003.11:g.197680895C>T , CM000665.1:g.197680895C>T	GRCh37
NC_000003.10:g.199165292C>T	NCBI36
NG_011743.1:g.8844C>T
NG_033072.1:g.10992G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265239.11:c.-60+5505G>A (IQCG) MANE Select	ENSP00000265239.6:n.-60+5505G>A
ENST00000448864.6:c.186C>T (RPL35A)	ENSP00000393393.1:p.Gly62=
ENST00000642387.1:n.377C>T (RPL35A)
ENST00000647248.2:c.186C>T (RPL35A) MANE Select	ENSP00000495672.1:p.Gly62=
ENST00000265239.10:c.-60+5505G>A (IQCG)	ENSP00000265239.6:n.-60+5505G>A
ENST00000329092.12:n.333C>T (RPL35A)
ENST00000416896.1:c.-50+5505G>A (IQCG)	ENSP00000406411.1:n.-50+5505G>A
ENST00000429437.5:c.*35C>T (RPL35A)	ENSP00000398058.1:n.*35C>T
ENST00000439255.1:c.*185C>T (RPL35A)	ENSP00000410683.1:n.*185C>T
ENST00000442341.5:c.186C>T (RPL35A)	ENSP00000387688.1:p.Gly62=
ENST00000448864.5:c.186C>T (RPL35A)	ENSP00000393393.1:p.Gly62=
ENST00000464167.5:c.186C>T (RPL35A)	ENSP00000419117.1:p.Gly62=
ENST00000474640.1:n.462C>T (RPL35A)
ENST00000480302.5:n.312+5505G>A (IQCG)
ENST00000485439.5:n.250C>T (RPL35A)
NM_000996.2:c.186C>T (RPL35A)	NP_000987.2:p.Gly62=
NM_001316311.1:c.186C>T (RPL35A)	NP_001303240.1:p.Gly62=
NM_032263.3:c.-60+5505G>A (IQCG)	NP_115639.1:n.-60+5505G>A
XR_924190.1:n.356+5505G>A (IQCG)
NM_000996.4:c.186C>T (RPL35A) MANE Select	NP_000987.2:p.Gly62=
NM_001323028.1:c.-50+5505G>A (IQCG)	NP_001309957.1:n.-50+5505G>A
NM_001323029.1:c.-375+5505G>A (IQCG)	NP_001309958.1:n.-375+5505G>A
NM_032263.4:c.-60+5505G>A (IQCG)	NP_115639.1:n.-60+5505G>A
XM_024453790.1:c.-60+5505G>A (IQCG)	XP_024309558.1:n.-60+5505G>A
XR_002959600.1:n.356+5505G>A (IQCG)
NM_032263.5:c.-60+5505G>A (IQCG) MANE Select	NP_115639.1:n.-60+5505G>A
NM_001316311.2:c.186C>T (RPL35A)	NP_001303240.1:p.Gly62=
NM_001323028.2:c.-50+5505G>A (IQCG)	NP_001309957.1:n.-50+5505G>A
NM_001323029.2:c.-375+5505G>A (IQCG)	NP_001309958.1:n.-375+5505G>A