Canonical Allele Identifier: CA6107555

Gene: RNASEH2C KAT5

Linked Data

• ClinVar Variation Id: 305342
• ClinVar RCV Id: RCV000316418
• dbSNP Id: rs201326733
• ExAC: 11:65486507 C / T
• gnomAD v2: 11-65486507-C-T
• gnomAD v3: 11-65719036-C-T
• gnomAD v4: 11-65719036-C-T
• MyVariant Identifiers: chr11:g.65486507C>T (hg19) ; chr11:g.65719036C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65719036C>T , CM000673.2:g.65719036C>T	GRCh38
NC_000011.9:g.65486507C>T , CM000673.1:g.65486507C>T	GRCh37
NC_000011.8:g.65243083C>T	NCBI36
NG_008976.2:g.6903G>A , LRG_280:g.6903G>A
NG_033057.1:g.12035C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308418.10:c.*747G>A (RNASEH2C) MANE Select	ENSP00000308193.5:n.*747G>A
ENST00000341318.9:c.1507-11C>T (KAT5) MANE Select	ENSP00000340330.4:n.1507-11C>T
ENST00000528220.2:n.1471G>A (RNASEH2C)
ENST00000531596.6:c.*223G>A (RNASEH2C)	ENSP00000435717.2:n.*223G>A
ENST00000534482.6:c.*747G>A (RNASEH2C)	ENSP00000432081.2:n.*747G>A
ENST00000642430.1:n.611G>A (RNASEH2C)
ENST00000643214.1:n.1316G>A (RNASEH2C)
ENST00000644142.1:c.*103-214G>A (RNASEH2C)	ENSP00000493695.1:n.*103-214G>A
ENST00000644198.1:n.494+645G>A (RNASEH2C)
ENST00000646597.1:n.534+645G>A (RNASEH2C)
ENST00000308418.8:c.*747G>A (RNASEH2C)	ENSP00000308193.4:n.*747G>A
ENST00000341318.8:c.1507-11C>T (KAT5)	ENSP00000340330.4:n.1507-11C>T
ENST00000352980.8:c.1252-11C>T (KAT5)	ENSP00000344955.4:n.1252-11C>T
ENST00000377046.7:c.1408-11C>T (KAT5)	ENSP00000366245.3:n.1408-11C>T
ENST00000525600.1:n.489-11C>T (KAT5)
ENST00000530446.5:c.1351-11C>T (KAT5)	ENSP00000434765.1:n.1351-11C>T
ENST00000531596.5:c.699G>A (RNASEH2C)
ENST00000533596.1:c.153-11C>T (KAT5)
ENST00000533698.5:c.477-267G>A (RNASEH2C)
ENST00000534482.5:c.491+645G>A (RNASEH2C)
ENST00000534650.5:c.775-11C>T (KAT5)	ENSP00000431819.1:n.775-11C>T
NM_001206833.1:c.1351-11C>T (KAT5)	NP_001193762.1:n.1351-11C>T
NM_006388.3:c.1408-11C>T (KAT5)	NP_006379.2:n.1408-11C>T
NM_032193.3:c.*747G>A , LRG_280t1:c.*747G>A (RNASEH2C)	NP_115569.2:n.*747G>A
NM_182709.2:c.1252-11C>T (KAT5)	NP_874368.1:n.1252-11C>T
NM_182710.2:c.1507-11C>T (KAT5)	NP_874369.1:n.1507-11C>T
XM_006718421.1:c.1435-11C>T (KAT5)	XP_006718484.1:n.1435-11C>T
XM_006718421.3:c.1435-11C>T (KAT5)	XP_006718484.1:n.1435-11C>T
XR_001747726.2:n.1689-11C>T (KAT5)
XR_001747727.2:n.1654-11C>T (KAT5)
XR_001747728.1:n.1370-11C>T (KAT5)
XR_002957116.1:n.3249-11C>T (KAT5)
NM_182710.3:c.1507-11C>T (KAT5) MANE Select	NP_874369.1:n.1507-11C>T
NM_001206833.2:c.1351-11C>T (KAT5)	NP_001193762.1:n.1351-11C>T
NM_006388.4:c.1408-11C>T (KAT5)	NP_006379.2:n.1408-11C>T
NM_032193.4:c.*747G>A (RNASEH2C) MANE Select	NP_115569.2:n.*747G>A
NM_182709.3:c.1252-11C>T (KAT5)	NP_874368.1:n.1252-11C>T