Canonical Allele Identifier: CA107691258
Gene: ZNF827 HGNC NCBI

Linked Data

dbSNP Id: rs2048161

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.145932013A>C , CM000666.2:g.145932013A>C GRCh38
NC_000004.11:g.146853165A>C , CM000666.1:g.146853165A>C GRCh37
NC_000004.10:g.147072615A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000379448.9:c.43+6352T>G ENSP00000368761.4:n.43+6352T>G
ENST00000503462.3:c.43+6352T>G ENSP00000424541.2:n.43+6352T>G
ENST00000508784.6:c.43+6352T>G MANE Select ENSP00000421863.1:n.43+6352T>G
ENST00000513840.2:c.43+6352T>G ENSP00000499867.1:n.43+6352T>G
ENST00000652097.1:c.43+6352T>G ENSP00000498532.1:n.43+6352T>G
ENST00000656985.1:c.43+6352T>G ENSP00000499364.1:n.43+6352T>G
ENST00000671699.1:n.154+4023T>G
ENST00000672123.1:n.132+6352T>G
ENST00000379448.8:c.43+6352T>G ENSP00000368761.4:n.43+6352T>G
ENST00000508784.5:c.43+6352T>G ENSP00000421863.1:n.43+6352T>G
ENST00000513320.5:c.43+6352T>G ENSP00000423130.1:n.43+6352T>G
NM_001306215.1:c.43+6352T>G NP_001293144.1:n.43+6352T>G
NM_178835.3:c.43+6352T>G NP_849157.2:n.43+6352T>G
NM_178835.4:c.43+6352T>G NP_849157.2:n.43+6352T>G
XM_011531634.1:c.43+6352T>G XP_011529936.1:n.43+6352T>G
XM_011531636.1:c.-94+6352T>G XP_011529938.1:n.-94+6352T>G
XM_011531634.3:c.43+6352T>G XP_011529936.1:n.43+6352T>G
XM_017007768.2:c.43+6352T>G XP_016863257.1:n.43+6352T>G
XM_017007770.2:c.43+6352T>G XP_016863259.1:n.43+6352T>G
XM_017007771.2:c.43+6352T>G XP_016863260.1:n.43+6352T>G
XM_017007772.2:c.43+6352T>G XP_016863261.1:n.43+6352T>G
XM_017007773.2:c.43+6352T>G XP_016863262.1:n.43+6352T>G
XM_017007774.2:c.43+6352T>G XP_016863263.1:n.43+6352T>G
XM_017007775.2:c.43+6352T>G XP_016863264.1:n.43+6352T>G
XM_017007776.2:c.43+6352T>G XP_016863265.1:n.43+6352T>G
XR_001741145.2:n.357+6352T>G
NM_001306215.2:c.43+6352T>G MANE Select NP_001293144.1:n.43+6352T>G
NM_178835.5:c.43+6352T>G NP_849157.2:n.43+6352T>G