Canonical Allele Identifier: CA1619212206

Gene: LTA

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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