Canonical Allele Identifier: CA360331836

Gene: AP3B1

Linked Data

• MyVariant Identifiers: chr5:g.77334867C>G (hg19) ; chr5:g.78039043C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.78039043C>G , CM000667.2:g.78039043C>G	GRCh38
NC_000005.9:g.77334867C>G , CM000667.1:g.77334867C>G	GRCh37
NC_000005.8:g.77370623C>G	NCBI36
NG_007268.1:g.260662G>C , LRG_170:g.260662G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519295.6:c.2662G>C	ENSP00000430597.1:p.Asp888His
ENST00000523204.2:n.609G>C
ENST00000695447.1:c.2702G>C	ENSP00000511917.1:n.2702G>C
ENST00000695450.1:c.2008G>C	ENSP00000511919.1:p.Asp670His
ENST00000695451.1:c.*2571G>C	ENSP00000511920.1:n.*2571G>C
ENST00000695453.1:c.2752G>C	ENSP00000511921.1:p.Asp918His
ENST00000695454.1:c.2803G>C	ENSP00000511922.1:p.Asp935His
ENST00000695455.1:c.2662G>C	ENSP00000511923.1:p.Asp888His
ENST00000695458.1:n.524G>C
ENST00000695488.1:c.2809G>C	ENSP00000511959.1:p.Asp937His
ENST00000695505.1:n.2967G>C
ENST00000695506.1:n.461G>C
ENST00000695507.1:c.*334G>C	ENSP00000511970.1:n.*334G>C
ENST00000695510.1:c.2809G>C	ENSP00000511973.1:p.Asp937His
ENST00000695511.1:c.2809G>C	ENSP00000511974.1:p.Asp937His
ENST00000695512.1:c.2629G>C	ENSP00000511975.1:p.Asp877His
ENST00000695513.1:c.2674G>C	ENSP00000511976.1:p.Asp892His
ENST00000695515.1:c.2809G>C	ENSP00000511978.1:p.Asp937His
ENST00000255194.11:c.2809G>C MANE Select	ENSP00000255194.7:p.Asp937His
ENST00000255194.10:c.2809G>C	ENSP00000255194.6:p.Asp937His
ENST00000519295.5:c.2662G>C	ENSP00000430597.1:p.Asp888His
ENST00000522901.1:c.108G>C
ENST00000523204.1:n.609G>C
NM_001271769.1:c.2662G>C	NP_001258698.1:p.Asp888His
NM_003664.4:c.2809G>C , LRG_170t1:c.2809G>C	NP_003655.3:p.Asp937His
XM_005248618.2:c.2809G>C	XP_005248675.1:p.Asp937His
XM_005248618.4:c.2809G>C	XP_005248675.1:p.Asp937His
XM_017010001.1:c.2662G>C	XP_016865490.1:p.Asp888His
NM_001271769.2:c.2662G>C	NP_001258698.1:p.Asp888His
NM_003664.5:c.2809G>C MANE Select	NP_003655.3:p.Asp937His