Canonical Allele Identifier: CA355902670

Gene: IQCG RPL35A

Linked Data

• MyVariant Identifiers: chr3:g.197678106A>C (hg19) ; chr3:g.197951235A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.197951235A>C , CM000665.2:g.197951235A>C	GRCh38
NC_000003.11:g.197678106A>C , CM000665.1:g.197678106A>C	GRCh37
NC_000003.10:g.199162503A>C	NCBI36
NG_011743.1:g.6055A>C
NG_033072.1:g.13781T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265239.11:c.-59-5549T>G (IQCG) MANE Select	ENSP00000265239.6:n.-59-5549T>G
ENST00000448864.6:c.88A>C (RPL35A)	ENSP00000393393.1:p.Ile30Leu
ENST00000642387.1:n.279A>C (RPL35A)
ENST00000647248.2:c.88A>C (RPL35A) MANE Select	ENSP00000495672.1:p.Ile30Leu
ENST00000265239.10:c.-59-5549T>G (IQCG)	ENSP00000265239.6:n.-59-5549T>G
ENST00000329092.12:n.149A>C (RPL35A)
ENST00000416896.1:c.-49-7184T>G (IQCG)	ENSP00000406411.1:n.-49-7184T>G
ENST00000429437.5:c.88A>C (RPL35A)	ENSP00000398058.1:p.Ile30Leu
ENST00000439255.1:c.88A>C (RPL35A)	ENSP00000410683.1:p.Ile30Leu
ENST00000442341.5:c.88A>C (RPL35A)	ENSP00000387688.1:p.Ile30Leu
ENST00000448864.5:c.88A>C (RPL35A)	ENSP00000393393.1:p.Ile30Leu
ENST00000464167.5:c.88A>C (RPL35A)	ENSP00000419117.1:p.Ile30Leu
ENST00000480302.5:n.313-5549T>G (IQCG)
ENST00000485439.5:n.152A>C (RPL35A)
ENST00000496582.5:n.149A>C (RPL35A)
NM_000996.2:c.88A>C (RPL35A)	NP_000987.2:p.Ile30Leu
NM_001316311.1:c.88A>C (RPL35A)	NP_001303240.1:p.Ile30Leu
NM_032263.3:c.-59-5549T>G (IQCG)	NP_115639.1:n.-59-5549T>G
XR_924190.1:n.357-5549T>G (IQCG)
NM_000996.4:c.88A>C (RPL35A) MANE Select	NP_000987.2:p.Ile30Leu
NM_001323028.1:c.-49-7184T>G (IQCG)	NP_001309957.1:n.-49-7184T>G
NM_001323029.1:c.-374-5549T>G (IQCG)	NP_001309958.1:n.-374-5549T>G
NM_032263.4:c.-59-5549T>G (IQCG)	NP_115639.1:n.-59-5549T>G
XM_024453790.1:c.-59-5549T>G (IQCG)	XP_024309558.1:n.-59-5549T>G
XR_002959600.1:n.357-5549T>G (IQCG)
NM_032263.5:c.-59-5549T>G (IQCG) MANE Select	NP_115639.1:n.-59-5549T>G
NM_001316311.2:c.88A>C (RPL35A)	NP_001303240.1:p.Ile30Leu
NM_001323028.2:c.-49-7184T>G (IQCG)	NP_001309957.1:n.-49-7184T>G
NM_001323029.2:c.-374-5549T>G (IQCG)	NP_001309958.1:n.-374-5549T>G