Canonical Allele Identifier: CA1947392837

Gene: AP2A2

Linked Data

• dbSNP Id: rs1853658516

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.941856G>T , CM000673.2:g.941856G>T	GRCh38
NC_000011.9:g.941856G>T , CM000673.1:g.941856G>T	GRCh37
NC_000011.8:g.931856G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000527024.2:c.49+962G>T	ENSP00000434563.2:n.49+962G>T
ENST00000528195.6:c.67+15768G>T	ENSP00000510810.1:n.67+15768G>T
ENST00000529818.6:c.-162+16919G>T	ENSP00000509792.1:n.-162+16919G>T
ENST00000529858.6:n.209+15768G>T
ENST00000531548.6:c.-162+9079G>T	ENSP00000433498.2:n.-162+9079G>T
ENST00000534328.6:c.-358-14930G>T	ENSP00000436059.2:n.-358-14930G>T
ENST00000534485.6:c.-162+8259G>T	ENSP00000435756.2:n.-162+8259G>T
ENST00000687792.1:c.67+15768G>T	ENSP00000508951.1:n.67+15768G>T
ENST00000687890.1:c.67+15768G>T	ENSP00000510756.1:n.67+15768G>T
ENST00000693238.1:c.67+15768G>T	ENSP00000510648.1:n.67+15768G>T
ENST00000448903.7:c.67+15768G>T MANE Select	ENSP00000413234.3:n.67+15768G>T
ENST00000332231.9:c.67+15768G>T	ENSP00000327694.5:n.67+15768G>T
ENST00000448903.6:c.67+15768G>T	ENSP00000413234.2:n.67+15768G>T
ENST00000525796.5:c.-46+15856G>T	ENSP00000437228.1:n.-46+15856G>T
ENST00000527024.1:c.49+962G>T	ENSP00000434563.1:n.49+962G>T
ENST00000528195.5:n.144+15768G>T
ENST00000528815.5:c.67+15768G>T	ENSP00000431630.1:n.67+15768G>T
ENST00000529818.5:n.44+16919G>T
ENST00000529858.5:n.220-14930G>T
ENST00000531548.5:c.85+9079G>T	ENSP00000433498.1:n.85+9079G>T
ENST00000534328.5:c.67+15768G>T	ENSP00000436059.1:n.67+15768G>T
ENST00000534485.5:c.37+8259G>T	ENSP00000435756.1:n.37+8259G>T
NM_001242837.1:c.67+15768G>T	NP_001229766.1:n.67+15768G>T
NM_012305.3:c.67+15768G>T	NP_036437.1:n.67+15768G>T
XM_011519929.1:c.-162+8259G>T	XP_011518231.1:n.-162+8259G>T
XM_011519930.1:c.67+15768G>T	XP_011518232.1:n.67+15768G>T
XR_930847.1:n.241+15768G>T
NR_144509.1:n.280+15768G>T
NR_144510.1:n.280+15768G>T
XM_011519930.3:c.67+15768G>T	XP_011518232.1:n.67+15768G>T
NM_012305.4:c.67+15768G>T MANE Select	NP_036437.1:n.67+15768G>T
NR_144509.2:n.219+15768G>T
NR_144510.2:n.219+15768G>T
NM_001242837.2:c.67+15768G>T	NP_001229766.1:n.67+15768G>T