Canonical Allele Identifier: CA10615484

Linked Data

ClinVar Variation Id: 344525
ClinVar RCV Id: RCV000394441
dbSNP Id: rs564722971

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.197950221G>A , CM000665.2:g.197950221G>A GRCh38
NC_000003.11:g.197677092G>A , CM000665.1:g.197677092G>A GRCh37
NC_000003.10:g.199161489G>A NCBI36
NG_011743.1:g.5041G>A
NG_033072.1:g.14795C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265239.11:c.-59-4535C>T (IQCG) MANE Select ENSP00000265239.6:n.-59-4535C>T
ENST00000448864.6:c.-111G>A (RPL35A) ENSP00000393393.1:n.-111G>A
ENST00000642148.1:n.30G>A (RPL35A)
ENST00000642387.1:n.31G>A (RPL35A)
ENST00000647248.2:c.-33G>A (RPL35A) MANE Select ENSP00000495672.1:n.-33G>A
ENST00000265239.10:c.-59-4535C>T (IQCG) ENSP00000265239.6:n.-59-4535C>T
ENST00000329092.12:n.29G>A (RPL35A)
ENST00000416896.1:c.-49-6170C>T (IQCG) ENSP00000406411.1:n.-49-6170C>T
ENST00000429437.5:c.-33G>A (RPL35A) ENSP00000398058.1:n.-33G>A
ENST00000448864.5:c.-111G>A (RPL35A) ENSP00000393393.1:n.-111G>A
ENST00000464167.5:c.-33G>A (RPL35A) ENSP00000419117.1:n.-33G>A
ENST00000480302.5:n.313-4535C>T (IQCG)
ENST00000485439.5:n.32G>A (RPL35A)
ENST00000496582.5:n.29G>A (RPL35A)
NM_000996.2:c.-33G>A (RPL35A) NP_000987.2:n.-33G>A
NM_032263.3:c.-59-4535C>T (IQCG) NP_115639.1:n.-59-4535C>T
XR_924190.1:n.357-4535C>T (IQCG)
NM_000996.4:c.-33G>A (RPL35A) MANE Select NP_000987.2:n.-33G>A
NM_001323028.1:c.-49-6170C>T (IQCG) NP_001309957.1:n.-49-6170C>T
NM_001323029.1:c.-374-4535C>T (IQCG) NP_001309958.1:n.-374-4535C>T
NM_032263.4:c.-59-4535C>T (IQCG) NP_115639.1:n.-59-4535C>T
XM_024453790.1:c.-59-4535C>T (IQCG) XP_024309558.1:n.-59-4535C>T
XR_002959600.1:n.357-4535C>T (IQCG)
NM_032263.5:c.-59-4535C>T (IQCG) MANE Select NP_115639.1:n.-59-4535C>T
NM_001316311.2:c.-111G>A (RPL35A) NP_001303240.1:n.-111G>A
NM_001323028.2:c.-49-6170C>T (IQCG) NP_001309957.1:n.-49-6170C>T
NM_001323029.2:c.-374-4535C>T (IQCG) NP_001309958.1:n.-374-4535C>T