Canonical Allele Identifier: CA345045021

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083180T>C (hg19) ; chr1:g.226895479T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895479T>C , CM000663.2:g.226895479T>C	GRCh38
NC_000001.10:g.227083180T>C , CM000663.1:g.227083180T>C	GRCh37
NC_000001.9:g.225149803T>C	NCBI36
NG_007381.1:g.29908T>C
NG_012825.2:g.2944T>C
NG_007381.2:g.30296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1247T>C	ENSP00000355741.2:p.Leu416Pro
ENST00000366782.6:c.1247T>C	ENSP00000355746.2:p.Leu416Pro
ENST00000366783.8:c.1247T>C MANE Select	ENSP00000355747.3:p.Leu416Pro
ENST00000471728.2:n.1885T>C
ENST00000524196.6:c.1247T>C	ENSP00000429036.2:p.Leu416Pro
ENST00000626989.3:c.1247T>C	ENSP00000486498.2:p.Leu416Pro
ENST00000676467.1:c.*1074T>C	ENSP00000504294.1:n.*1074T>C
ENST00000676747.1:c.1188+1354T>C	ENSP00000503244.1:n.1188+1354T>C
ENST00000676884.1:c.1247T>C	ENSP00000503200.1:p.Leu416Pro
ENST00000676888.1:c.*588T>C	ENSP00000504483.1:n.*588T>C
ENST00000676907.1:c.*826T>C	ENSP00000504410.1:n.*826T>C
ENST00000676945.1:c.1191+1354T>C	ENSP00000504433.1:n.1191+1354T>C
ENST00000677065.1:n.1808T>C
ENST00000677414.1:c.1247T>C	ENSP00000503116.1:p.Leu416Pro
ENST00000677529.1:n.2977T>C
ENST00000677596.1:c.*1469T>C	ENSP00000503618.1:n.*1469T>C
ENST00000677599.1:c.1191+1354T>C	ENSP00000503673.1:n.1191+1354T>C
ENST00000677748.1:n.3502T>C
ENST00000677880.1:c.812T>C	ENSP00000503121.1:p.Leu271Pro
ENST00000678021.1:c.*870T>C	ENSP00000504674.1:n.*870T>C
ENST00000678233.1:c.1247T>C	ENSP00000504728.1:p.Leu416Pro
ENST00000678320.1:c.1148T>C	ENSP00000503680.1:p.Leu383Pro
ENST00000678655.1:c.1092+1354T>C	ENSP00000504230.1:n.1092+1354T>C
ENST00000678706.1:c.*624T>C	ENSP00000503659.1:n.*624T>C
ENST00000678776.1:c.*1384T>C	ENSP00000504624.1:n.*1384T>C
ENST00000678784.1:c.1073-2241T>C	ENSP00000504652.1:n.1073-2241T>C
ENST00000678820.1:c.1089+1354T>C	ENSP00000504138.1:n.1089+1354T>C
ENST00000678835.1:c.*757-2241T>C	ENSP00000504343.1:n.*757-2241T>C
ENST00000679088.1:c.1247T>C	ENSP00000504727.1:p.Leu416Pro
ENST00000679098.1:c.1247T>C	ENSP00000504303.1:p.Leu416Pro
ENST00000366782.5:c.1346T>C	ENSP00000355746.1:p.Leu449Pro
ENST00000366783.7:c.1247T>C	ENSP00000355747.3:p.Leu416Pro
ENST00000422240.6:c.1244T>C	ENSP00000403737.2:p.Leu415Pro
ENST00000471728.1:n.505T>C
ENST00000472139.2:c.815T>C	ENSP00000427806.1:p.Leu272Pro
ENST00000626989.2:c.1346T>C	ENSP00000486498.1:p.Leu449Pro
NM_000447.2:c.1247T>C	NP_000438.2:p.Leu416Pro
NM_012486.2:c.1244T>C	NP_036618.2:p.Leu415Pro
XM_005273199.2:c.1247T>C	XP_005273256.1:p.Leu416Pro
XM_011544236.1:c.815T>C	XP_011542538.1:p.Leu272Pro
XR_949149.1:n.1981T>C
XM_005273199.4:c.1247T>C	XP_005273256.1:p.Leu416Pro
XM_017001835.1:c.1247T>C	XP_016857324.1:p.Leu416Pro
XM_017001836.1:c.1244T>C	XP_016857325.1:p.Leu415Pro
XR_001737316.2:n.1478-2241T>C
XR_001737317.2:n.1478-2241T>C
XR_001737318.2:n.1962T>C
XR_001737319.1:n.2305T>C
XR_001737320.1:n.2302T>C
XR_001737321.1:n.1797T>C
XR_949149.2:n.1959T>C
XR_949150.3:n.2178T>C
NM_000447.3:c.1247T>C MANE Select	NP_000438.2:p.Leu416Pro
NM_012486.3:c.1244T>C	NP_036618.2:p.Leu415Pro