Canonical Allele Identifier: CA1619212415

Gene: LTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31573021G= , CM000668.2:g.31573021G=	GRCh38
NC_000006.11:g.31540798G= , CM000668.1:g.31540798G=	GRCh37
NC_000006.10:g.31648777G=	NCBI36
NG_007462.1:g.2449G=
NG_012010.1:g.5923G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000418386.3:c.193G= MANE Select	ENSP00000413450.2:p.Ala65=
ENST00000418386.2:c.193G=	ENSP00000413450.2:p.Ala65=
ENST00000454783.5:c.193G=	ENSP00000403495.1:p.Ala65=
ENST00000471842.1:n.441G=
ENST00000489638.5:n.321G=
NM_000595.3:c.193G=	NP_000586.2:p.Ala65=
NM_001159740.2:c.193G=	NP_001153212.1:p.Ala65=
XM_011514614.1:c.193G=	XP_011512916.1:p.Ala65=
XM_011514615.1:c.193G=	XP_011512917.1:p.Ala65=
XM_011514616.1:c.193G=	XP_011512918.1:p.Ala65=
XM_011514617.1:c.193G=	XP_011512919.1:p.Ala65=
XM_011514618.1:c.193G=	XP_011512920.1:p.Ala65=
XM_011514615.2:c.193G=	XP_011512917.1:p.Ala65=
XM_011514616.2:c.193G=	XP_011512918.1:p.Ala65=
XM_011514617.2:c.193G=	XP_011512919.1:p.Ala65=
NM_000595.4:c.193G= MANE Select	NP_000586.2:p.Ala65=