Canonical Allele Identifier: CA2789126

Gene: IQCG RPL35A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.197950934A>T , CM000665.2:g.197950934A>T	GRCh38
NC_000003.11:g.197677805A>T , CM000665.1:g.197677805A>T	GRCh37
NC_000003.10:g.199162202A>T	NCBI36
NG_011743.1:g.5754A>T
NG_033072.1:g.14082T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265239.11:c.-59-5248T>A (IQCG) MANE Select	ENSP00000265239.6:n.-59-5248T>A
ENST00000448864.6:c.-32-2A>T (RPL35A)	ENSP00000393393.1:n.-32-2A>T
ENST00000642387.1:n.202+51A>T (RPL35A)
ENST00000647248.2:c.-32-2A>T (RPL35A) MANE Select	ENSP00000495672.1:n.-32-2A>T
ENST00000265239.10:c.-59-5248T>A (IQCG)	ENSP00000265239.6:n.-59-5248T>A
ENST00000329092.12:n.30-2A>T (RPL35A)
ENST00000416896.1:c.-49-6883T>A (IQCG)	ENSP00000406411.1:n.-49-6883T>A
ENST00000429437.5:c.-32-2A>T (RPL35A)	ENSP00000398058.1:n.-32-2A>T
ENST00000442341.5:c.-32-2A>T (RPL35A)	ENSP00000387688.1:n.-32-2A>T
ENST00000448864.5:c.-32-2A>T (RPL35A)	ENSP00000393393.1:n.-32-2A>T
ENST00000464167.5:c.-32-2A>T (RPL35A)	ENSP00000419117.1:n.-32-2A>T
ENST00000480302.5:n.313-5248T>A (IQCG)
ENST00000485439.5:n.33-2A>T (RPL35A)
ENST00000496582.5:n.30-2A>T (RPL35A)
NM_000996.2:c.-32-2A>T (RPL35A)	NP_000987.2:n.-32-2A>T
NM_001316311.1:c.-32-2A>T (RPL35A)	NP_001303240.1:n.-32-2A>T
NM_032263.3:c.-59-5248T>A (IQCG)	NP_115639.1:n.-59-5248T>A
XR_924190.1:n.357-5248T>A (IQCG)
NM_000996.4:c.-32-2A>T (RPL35A) MANE Select	NP_000987.2:n.-32-2A>T
NM_001323028.1:c.-49-6883T>A (IQCG)	NP_001309957.1:n.-49-6883T>A
NM_001323029.1:c.-374-5248T>A (IQCG)	NP_001309958.1:n.-374-5248T>A
NM_032263.4:c.-59-5248T>A (IQCG)	NP_115639.1:n.-59-5248T>A
XM_024453790.1:c.-59-5248T>A (IQCG)	XP_024309558.1:n.-59-5248T>A
XR_002959600.1:n.357-5248T>A (IQCG)
NM_032263.5:c.-59-5248T>A (IQCG) MANE Select	NP_115639.1:n.-59-5248T>A
NM_001316311.2:c.-32-2A>T (RPL35A)	NP_001303240.1:n.-32-2A>T
NM_001323028.2:c.-49-6883T>A (IQCG)	NP_001309957.1:n.-49-6883T>A
NM_001323029.2:c.-374-5248T>A (IQCG)	NP_001309958.1:n.-374-5248T>A