Canonical Allele Identifier: CA1143428620

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226896103G= , CM000663.2:g.226896103G=	GRCh38
NC_000001.10:g.227083804G= , CM000663.1:g.227083804G=	GRCh37
NC_000001.9:g.225150427G=	NCBI36
NG_007381.1:g.30532G=
NG_012825.2:g.3568G=
NG_007381.2:g.30920G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*524G=	ENSP00000355741.2:n.*524G=
ENST00000524196.6:c.*524G=	ENSP00000429036.2:n.*524G=
ENST00000676747.1:c.1189-1617G=	ENSP00000503244.1:n.1189-1617G=
ENST00000676884.1:c.*524G=	ENSP00000503200.1:n.*524G=
ENST00000676945.1:c.1191+1978G=	ENSP00000504433.1:n.1191+1978G=
ENST00000677599.1:c.1191+1978G=	ENSP00000503673.1:n.1191+1978G=
ENST00000678233.1:c.*8+516G=	ENSP00000504728.1:n.*8+516G=
ENST00000678655.1:c.1093-1617G=	ENSP00000504230.1:n.1093-1617G=
ENST00000678784.1:c.1073-1617G=	ENSP00000504652.1:n.1073-1617G=
ENST00000678820.1:c.1090-1617G=	ENSP00000504138.1:n.1090-1617G=
ENST00000678835.1:c.*757-1617G=	ENSP00000504343.1:n.*757-1617G=
ENST00000679098.1:c.*8+516G=	ENSP00000504303.1:n.*8+516G=
ENST00000626989.2:c.1970G=	ENSP00000486498.1:n.1970G=
NM_000447.2:c.*524G=	NP_000438.2:n.*524G=
NM_012486.2:c.*524G=	NP_036618.2:n.*524G=
XM_005273199.2:c.*524G=	XP_005273256.1:n.*524G=
XM_011544236.1:c.*524G=	XP_011542538.1:n.*524G=
XM_005273199.4:c.*524G=	XP_005273256.1:n.*524G=
XM_017001835.1:c.*524G=	XP_016857324.1:n.*524G=
XM_017001836.1:c.*524G=	XP_016857325.1:n.*524G=
XR_001737316.2:n.1478-1617G=
XR_001737317.2:n.1478-1617G=
XR_001737318.2:n.2586G=
XR_001737319.1:n.2929G=
XR_001737320.1:n.2926G=
XR_001737321.1:n.2421G=
XR_949149.2:n.2583G=
XR_949150.3:n.2802G=