Canonical Allele Identifier: CA788589726

Gene: ZNF827

Linked Data

• dbSNP Id: rs1214596379
• gnomAD v3: 4-145931943-A-G
• gnomAD v4: 4-145931943-A-G
• MyVariant Identifiers: chr4:g.146853095A>G (hg19) ; chr4:g.145931943A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145931943A>G , CM000666.2:g.145931943A>G	GRCh38
NC_000004.11:g.146853095A>G , CM000666.1:g.146853095A>G	GRCh37
NC_000004.10:g.147072545A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379448.9:c.43+6422T>C	ENSP00000368761.4:n.43+6422T>C
ENST00000503462.3:c.43+6422T>C	ENSP00000424541.2:n.43+6422T>C
ENST00000508784.6:c.43+6422T>C MANE Select	ENSP00000421863.1:n.43+6422T>C
ENST00000513840.2:c.43+6422T>C	ENSP00000499867.1:n.43+6422T>C
ENST00000652097.1:c.43+6422T>C	ENSP00000498532.1:n.43+6422T>C
ENST00000656985.1:c.43+6422T>C	ENSP00000499364.1:n.43+6422T>C
ENST00000671699.1:n.154+4093T>C
ENST00000672123.1:n.132+6422T>C
ENST00000379448.8:c.43+6422T>C	ENSP00000368761.4:n.43+6422T>C
ENST00000508784.5:c.43+6422T>C	ENSP00000421863.1:n.43+6422T>C
ENST00000513320.5:c.43+6422T>C	ENSP00000423130.1:n.43+6422T>C
NM_001306215.1:c.43+6422T>C	NP_001293144.1:n.43+6422T>C
NM_178835.3:c.43+6422T>C	NP_849157.2:n.43+6422T>C
NM_178835.4:c.43+6422T>C	NP_849157.2:n.43+6422T>C
XM_011531634.1:c.43+6422T>C	XP_011529936.1:n.43+6422T>C
XM_011531636.1:c.-94+6422T>C	XP_011529938.1:n.-94+6422T>C
XM_011531634.3:c.43+6422T>C	XP_011529936.1:n.43+6422T>C
XM_017007768.2:c.43+6422T>C	XP_016863257.1:n.43+6422T>C
XM_017007770.2:c.43+6422T>C	XP_016863259.1:n.43+6422T>C
XM_017007771.2:c.43+6422T>C	XP_016863260.1:n.43+6422T>C
XM_017007772.2:c.43+6422T>C	XP_016863261.1:n.43+6422T>C
XM_017007773.2:c.43+6422T>C	XP_016863262.1:n.43+6422T>C
XM_017007774.2:c.43+6422T>C	XP_016863263.1:n.43+6422T>C
XM_017007775.2:c.43+6422T>C	XP_016863264.1:n.43+6422T>C
XM_017007776.2:c.43+6422T>C	XP_016863265.1:n.43+6422T>C
XR_001741145.2:n.357+6422T>C
NM_001306215.2:c.43+6422T>C MANE Select	NP_001293144.1:n.43+6422T>C
NM_178835.5:c.43+6422T>C	NP_849157.2:n.43+6422T>C