Canonical Allele Identifier: CA1144978118
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235806790C= , CM000663.2:g.235806790C= GRCh38
NC_000001.10:g.235970090C= , CM000663.1:g.235970090C= GRCh37
NC_000001.9:g.234036713C= NCBI36
NG_007397.1:g.81851G= , LRG_143:g.81851G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697178.1:c.2364-18G= ENSP00000513163.1:n.2364-18G=
ENST00000697242.1:c.1767-18G= ENSP00000513207.1:n.1767-18G=
ENST00000389793.7:c.2364-18G= MANE Select ENSP00000374443.2:n.2364-18G=
ENST00000389793.6:c.2364-18G= ENSP00000374443.2:n.2364-18G=
ENST00000389794.7:c.2364-18G= ENSP00000374444.4:n.2364-18G=
ENST00000465349.5:n.2915-18G=
ENST00000489585.5:n.2915-18G=
NM_000081.3:c.2364-18G= , LRG_143t1:c.2364-18G= NP_000072.2:n.2364-18G=
NM_001301365.1:c.2364-18G= , LRG_143t2:c.2364-18G= NP_001288294.1:n.2364-18G=
XM_011544031.1:c.2364-18G= XP_011542333.1:n.2364-18G=
XM_011544032.1:c.2364-18G= XP_011542334.1:n.2364-18G=
XM_011544033.1:c.2364-18G= XP_011542335.1:n.2364-18G=
XM_011544034.1:c.2364-18G= XP_011542336.1:n.2364-18G=
XM_011544035.1:c.2364-18G= XP_011542337.1:n.2364-18G=
XM_011544036.1:c.27-18G= XP_011542338.1:n.27-18G=
XM_011544037.1:c.2364-18G= XP_011542339.1:n.2364-18G=
XM_011544038.1:c.2364-18G= XP_011542340.1:n.2364-18G=
XM_011544039.1:c.2364-18G= XP_011542341.1:n.2364-18G=
XM_011544040.1:c.2364-18G= XP_011542342.1:n.2364-18G=
XM_011544033.2:c.2364-18G= XP_011542335.1:n.2364-18G=
XM_011544035.2:c.2364-18G= XP_011542337.1:n.2364-18G=
XM_011544036.2:c.27-18G= XP_011542338.1:n.27-18G=
XM_011544037.2:c.2364-18G= XP_011542339.1:n.2364-18G=
XM_011544039.2:c.2364-18G= XP_011542341.1:n.2364-18G=
XM_017000150.1:c.2364-18G= XP_016855639.1:n.2364-18G=
XM_017000151.1:c.2364-18G= XP_016855640.1:n.2364-18G=
XR_001736946.2:n.2546-18G=
XR_001736947.1:n.2546-18G=
XR_001736948.1:n.2546-18G=
XR_002959252.1:n.2546-18G=
NM_000081.4:c.2364-18G= MANE Select NP_000072.2:n.2364-18G=