Canonical Allele Identifier: CA1087470154

Gene: LTA

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31572364A>T , CM000668.2:g.31572364A>T	GRCh38
NC_000006.11:g.31540141A>T , CM000668.1:g.31540141A>T	GRCh37
NC_000006.10:g.31648120A>T	NCBI36
NG_007462.1:g.1792A>T
NG_012010.1:g.5266A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418386.3:c.-92A>T MANE Select	ENSP00000413450.2:n.-92A>T
ENST00000418386.2:c.-92A>T	ENSP00000413450.2:n.-92A>T
ENST00000454783.5:c.-10+62A>T	ENSP00000403495.1:n.-10+62A>T
ENST00000471842.1:n.71A>T
ENST00000489638.5:n.33+62A>T
NM_000595.3:c.-92A>T	NP_000586.2:n.-92A>T
NM_001159740.2:c.-10+62A>T	NP_001153212.1:n.-10+62A>T
XM_011514614.1:c.-10+62A>T	XP_011512916.1:n.-10+62A>T
XM_011514615.1:c.-10+62A>T	XP_011512917.1:n.-10+62A>T
XM_011514616.1:c.-10+62A>T	XP_011512918.1:n.-10+62A>T
XM_011514617.1:c.-10+62A>T	XP_011512919.1:n.-10+62A>T
XM_011514618.1:c.-10+62A>T	XP_011512920.1:n.-10+62A>T
XR_926695.1:n.116+219T>A
NR_149045.1:n.121+219T>A
XM_011514615.2:c.-10+62A>T	XP_011512917.1:n.-10+62A>T
XM_011514616.2:c.-10+62A>T	XP_011512918.1:n.-10+62A>T
XM_011514617.2:c.-10+62A>T	XP_011512919.1:n.-10+62A>T
NM_000595.4:c.-92A>T MANE Select	NP_000586.2:n.-92A>T