Canonical Allele Identifier: CA50489782

Gene: HTRA2 LOXL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74532893G>A , CM000664.2:g.74532893G>A	GRCh38
NC_000002.11:g.74760020G>A , CM000664.1:g.74760020G>A	GRCh37
NC_000002.10:g.74613528G>A	NCBI36
NG_012163.1:g.8489G>A
NG_033037.1:g.1955C>T
NG_033047.1:g.26043C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437202.2:c.1219G>A (HTRA2)	ENSP00000399166.2:p.Glu407Lys
ENST00000462909.6:n.1035G>A (HTRA2)
ENST00000465521.2:n.1094G>A (HTRA2)
ENST00000467961.6:n.1019G>A (HTRA2)
ENST00000484881.6:n.910G>A (HTRA2)
ENST00000696725.1:n.1168G>A (HTRA2)
ENST00000696726.1:n.817G>A (HTRA2)
ENST00000696727.1:c.1189G>A (HTRA2)	ENSP00000512836.1:p.Glu397Lys
ENST00000696728.1:c.*192G>A (HTRA2)	ENSP00000512837.1:n.*192G>A
ENST00000696729.1:n.1348G>A (HTRA2)
ENST00000696731.1:n.1357G>A (HTRA2)
ENST00000258080.8:c.1285G>A (HTRA2) MANE Select	ENSP00000258080.3:p.Glu429Lys
ENST00000264094.8:c.*713C>T (LOXL3) MANE Select	ENSP00000264094.3:n.*713C>T
ENST00000258080.7:c.1285G>A (HTRA2)	ENSP00000258080.3:p.Glu429Lys
ENST00000264094.7:c.*713C>T (LOXL3)	ENSP00000264094.3:n.*713C>T
ENST00000352222.7:c.994G>A (HTRA2)	ENSP00000312893.3:p.Glu332Lys
ENST00000409249.5:c.*713C>T (LOXL3)	ENSP00000387103.1:n.*713C>T
ENST00000437202.1:c.1180G>A (HTRA2)	ENSP00000399166.1:p.Glu394Lys
ENST00000462909.5:n.1035G>A (HTRA2)
ENST00000467961.5:n.969G>A (HTRA2)
ENST00000470907.6:n.2358C>T (LOXL3)
ENST00000484352.5:n.1348G>A (HTRA2)
NM_001289164.1:c.*713C>T (LOXL3)	NP_001276093.1:n.*713C>T
NM_001289165.1:c.*713C>T (LOXL3)	NP_001276094.1:n.*713C>T
NM_013247.4:c.1285G>A (HTRA2)	NP_037379.1:p.Glu429Lys
NM_032603.3:c.*713C>T (LOXL3)	NP_115992.1:n.*713C>T
NM_145074.2:c.994G>A (HTRA2)	NP_659540.1:p.Glu332Lys
XM_005264266.2:c.1189G>A (HTRA2)	XP_005264323.1:p.Glu397Lys
NM_001289164.2:c.*713C>T (LOXL3)	NP_001276093.1:n.*713C>T
NM_001321727.1:c.1219G>A (HTRA2)	NP_001308656.1:p.Glu407Lys
NM_001321728.1:c.1189G>A (HTRA2)	NP_001308657.1:p.Glu397Lys
NM_032603.4:c.*713C>T (LOXL3)	NP_115992.1:n.*713C>T
NR_135769.1:n.1927G>A (HTRA2)
NR_135770.1:n.1355G>A (HTRA2)
NR_135771.1:n.1339G>A (HTRA2)
NR_135772.1:n.1359G>A (HTRA2)
NM_032603.5:c.*713C>T (LOXL3) MANE Select	NP_115992.1:n.*713C>T
NM_001289164.3:c.*713C>T (LOXL3)	NP_001276093.1:n.*713C>T
NM_001289165.2:c.*713C>T (LOXL3)	NP_001276094.1:n.*713C>T
NM_013247.5:c.1285G>A (HTRA2) MANE Select	NP_037379.1:p.Glu429Lys