Canonical Allele Identifier: CA823889215
Gene: LTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31572652C>T , CM000668.2:g.31572652C>T GRCh38
NC_000006.11:g.31540429C>T , CM000668.1:g.31540429C>T GRCh37
NC_000006.10:g.31648408C>T NCBI36
NG_007462.1:g.2080C>T
NG_012010.1:g.5554C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000418386.3:c.-9-82C>T MANE Select ENSP00000413450.2:n.-9-82C>T
ENST00000418386.2:c.-9-82C>T ENSP00000413450.2:n.-9-82C>T
ENST00000454783.5:c.-9-82C>T ENSP00000403495.1:n.-9-82C>T
ENST00000471842.1:n.154-82C>T
ENST00000489638.5:n.34-82C>T
NM_000595.3:c.-9-82C>T NP_000586.2:n.-9-82C>T
NM_001159740.2:c.-9-82C>T NP_001153212.1:n.-9-82C>T
XM_011514614.1:c.-9-82C>T XP_011512916.1:n.-9-82C>T
XM_011514615.1:c.-9-82C>T XP_011512917.1:n.-9-82C>T
XM_011514616.1:c.-9-82C>T XP_011512918.1:n.-9-82C>T
XM_011514617.1:c.-9-82C>T XP_011512919.1:n.-9-82C>T
XM_011514618.1:c.-9-82C>T XP_011512920.1:n.-9-82C>T
XR_926695.1:n.47G>A
NR_149045.1:n.52G>A
XM_011514615.2:c.-9-82C>T XP_011512917.1:n.-9-82C>T
XM_011514616.2:c.-9-82C>T XP_011512918.1:n.-9-82C>T
XM_011514617.2:c.-9-82C>T XP_011512919.1:n.-9-82C>T
NM_000595.4:c.-9-82C>T MANE Select NP_000586.2:n.-9-82C>T