Canonical Allele Identifier: CA1619212112

Gene: LTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31572294G= , CM000668.2:g.31572294G=	GRCh38
NC_000006.11:g.31540071G= , CM000668.1:g.31540071G=	GRCh37
NC_000006.10:g.31648050G=	NCBI36
NG_007462.1:g.1722G=
NG_012010.1:g.5196G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000595.4:c.-162G= MANE Select	NP_000586.2:n.-162G=
ENST00000418386.3:c.-162G= MANE Select	ENSP00000413450.2:n.-162G=
NM_000595.3:c.-162G=	NP_000586.2:n.-162G=
NM_001159740.2:c.-18G=	NP_001153212.1:n.-18G=
NR_149045.1:n.121+289C=
ENST00000418386.2:c.-162G=	ENSP00000413450.2:n.-162G=
ENST00000454783.5:c.-18G=	ENSP00000403495.1:n.-18G=
ENST00000471842.1:n.1G=
ENST00000489638.5:n.25G=
XM_011514614.1:c.-18G=	XP_011512916.1:n.-18G=
XM_011514615.1:c.-18G=	XP_011512917.1:n.-18G=
XM_011514615.2:c.-18G=	XP_011512917.1:n.-18G=
XM_011514616.1:c.-18G=	XP_011512918.1:n.-18G=
XM_011514616.2:c.-18G=	XP_011512918.1:n.-18G=
XM_011514617.1:c.-18G=	XP_011512919.1:n.-18G=
XM_011514617.2:c.-18G=	XP_011512919.1:n.-18G=
XM_011514618.1:c.-18G=	XP_011512920.1:n.-18G=
XR_926695.1:n.116+289C=