Canonical Allele Identifier: CA1619212205

Gene: LTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31572536A= , CM000668.2:g.31572536A=	GRCh38
NC_000006.11:g.31540313A= , CM000668.1:g.31540313A=	GRCh37
NC_000006.10:g.31648292A=	NCBI36
NG_007462.1:g.1964A=
NG_012010.1:g.5438A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000595.4:c.-10+90A= MANE Select	NP_000586.2:n.-10+90A=
ENST00000418386.3:c.-10+90A= MANE Select	ENSP00000413450.2:n.-10+90A=
NM_000595.3:c.-10+90A=	NP_000586.2:n.-10+90A=
NM_001159740.2:c.-9-198A=	NP_001153212.1:n.-9-198A=
NR_149045.1:n.121+47T=
ENST00000418386.2:c.-10+90A=	ENSP00000413450.2:n.-10+90A=
ENST00000454783.5:c.-9-198A=	ENSP00000403495.1:n.-9-198A=
ENST00000471842.1:n.153+90A=
ENST00000489638.5:n.34-198A=
XM_011514614.1:c.-9-198A=	XP_011512916.1:n.-9-198A=
XM_011514615.1:c.-9-198A=	XP_011512917.1:n.-9-198A=
XM_011514615.2:c.-9-198A=	XP_011512917.1:n.-9-198A=
XM_011514616.1:c.-9-198A=	XP_011512918.1:n.-9-198A=
XM_011514616.2:c.-9-198A=	XP_011512918.1:n.-9-198A=
XM_011514617.1:c.-9-198A=	XP_011512919.1:n.-9-198A=
XM_011514617.2:c.-9-198A=	XP_011512919.1:n.-9-198A=
XM_011514618.1:c.-9-198A=	XP_011512920.1:n.-9-198A=
XR_926695.1:n.116+47T=