Canonical Allele Identifier: CA1619212414

Gene: LTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31573020T= , CM000668.2:g.31573020T=	GRCh38
NC_000006.11:g.31540797T= , CM000668.1:g.31540797T=	GRCh37
NC_000006.10:g.31648776T=	NCBI36
NG_007462.1:g.2448T=
NG_012010.1:g.5922T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000418386.3:c.192T= MANE Select	ENSP00000413450.2:p.Ala64=
ENST00000418386.2:c.192T=	ENSP00000413450.2:p.Ala64=
ENST00000454783.5:c.192T=	ENSP00000403495.1:p.Ala64=
ENST00000471842.1:n.440T=
ENST00000489638.5:n.320T=
NM_000595.3:c.192T=	NP_000586.2:p.Ala64=
NM_001159740.2:c.192T=	NP_001153212.1:p.Ala64=
XM_011514614.1:c.192T=	XP_011512916.1:p.Ala64=
XM_011514615.1:c.192T=	XP_011512917.1:p.Ala64=
XM_011514616.1:c.192T=	XP_011512918.1:p.Ala64=
XM_011514617.1:c.192T=	XP_011512919.1:p.Ala64=
XM_011514618.1:c.192T=	XP_011512920.1:p.Ala64=
XM_011514615.2:c.192T=	XP_011512917.1:p.Ala64=
XM_011514616.2:c.192T=	XP_011512918.1:p.Ala64=
XM_011514617.2:c.192T=	XP_011512919.1:p.Ala64=
NM_000595.4:c.192T= MANE Select	NP_000586.2:p.Ala64=