Canonical Allele Identifier: CA363339244
Gene: LTA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31573014A>C , CM000668.2:g.31573014A>C GRCh38
NC_000006.11:g.31540791A>C , CM000668.1:g.31540791A>C GRCh37
NC_000006.10:g.31648770A>C NCBI36
NG_007462.1:g.2442A>C
NG_012010.1:g.5916A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000418386.3:c.186A>C MANE Select ENSP00000413450.2:p.Lys62Asn
ENST00000418386.2:c.186A>C ENSP00000413450.2:p.Lys62Asn
ENST00000454783.5:c.186A>C ENSP00000403495.1:p.Lys62Asn
ENST00000471842.1:n.434A>C
ENST00000489638.5:n.314A>C
NM_000595.3:c.186A>C NP_000586.2:p.Lys62Asn
NM_001159740.2:c.186A>C NP_001153212.1:p.Lys62Asn
XM_011514614.1:c.186A>C XP_011512916.1:p.Lys62Asn
XM_011514615.1:c.186A>C XP_011512917.1:p.Lys62Asn
XM_011514616.1:c.186A>C XP_011512918.1:p.Lys62Asn
XM_011514617.1:c.186A>C XP_011512919.1:p.Lys62Asn
XM_011514618.1:c.186A>C XP_011512920.1:p.Lys62Asn
XM_011514615.2:c.186A>C XP_011512917.1:p.Lys62Asn
XM_011514616.2:c.186A>C XP_011512918.1:p.Lys62Asn
XM_011514617.2:c.186A>C XP_011512919.1:p.Lys62Asn
NM_000595.4:c.186A>C MANE Select NP_000586.2:p.Lys62Asn