Canonical Allele Identifier: CA344940893

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235716727A>C , CM000663.2:g.235716727A>C	GRCh38
NC_000001.10:g.235880027A>C , CM000663.1:g.235880027A>C	GRCh37
NC_000001.9:g.233946650A>C	NCBI36
NG_007397.1:g.171914T>G , LRG_143:g.171914T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.9612T>G MANE Select	NP_000072.2:p.Tyr3204Ter
ENST00000389793.7:c.9612T>G MANE Select	ENSP00000374443.2:p.Tyr3204Ter
NM_000081.3:c.9612T>G , LRG_143t1:c.9612T>G	NP_000072.2:p.Tyr3204Ter
NM_001301365.1:c.9612T>G , LRG_143t2:c.9612T>G	NP_001288294.1:p.Tyr3204Ter
ENST00000389793.6:c.9612T>G	ENSP00000374443.2:p.Tyr3204Ter
ENST00000389794.7:c.*5036T>G	ENSP00000374444.4:n.*5036T>G
ENST00000461526.2:c.5140T>G	ENSP00000513165.1:n.5140T>G
ENST00000473037.5:n.4602T>G
ENST00000475277.1:n.478T>G
ENST00000475277.2:c.1707T>G	ENSP00000513164.1:p.Tyr569Ter
ENST00000697178.1:c.*5307T>G	ENSP00000513163.1:n.*5307T>G
ENST00000697235.1:c.162T>G	ENSP00000513202.1:p.Tyr54Ter
ENST00000697236.1:c.3076T>G	ENSP00000513203.1:n.3076T>G
ENST00000697237.1:c.568T>G
ENST00000697240.1:c.1746T>G	ENSP00000513205.1:p.Tyr582Ter
ENST00000697241.1:c.4092T>G	ENSP00000513206.1:p.Tyr1364Ter
XM_011544031.1:c.9774T>G	XP_011542333.1:p.Tyr3258Ter
XM_011544032.1:c.9774T>G	XP_011542334.1:p.Tyr3258Ter
XM_011544033.1:c.9774T>G	XP_011542335.1:p.Tyr3258Ter
XM_011544033.2:c.9774T>G	XP_011542335.1:p.Tyr3258Ter
XM_011544034.1:c.9636T>G	XP_011542336.1:p.Tyr3212Ter
XM_011544035.1:c.9774T>G	XP_011542337.1:p.Tyr3258Ter
XM_011544035.2:c.9774T>G	XP_011542337.1:p.Tyr3258Ter
XM_011544036.1:c.7437T>G	XP_011542338.1:p.Tyr2479Ter
XM_011544036.2:c.7437T>G	XP_011542338.1:p.Tyr2479Ter
XM_017000150.1:c.9774T>G	XP_016855639.1:p.Tyr3258Ter
XR_001736947.1:n.10647T>G