Canonical Allele Identifier: CA363339272

Gene: LTA

Linked Data

• MyVariant Identifiers: chr6:g.31540796C>A (hg19) ; chr6:g.31573019C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31573019C>A , CM000668.2:g.31573019C>A	GRCh38
NC_000006.11:g.31540796C>A , CM000668.1:g.31540796C>A	GRCh37
NC_000006.10:g.31648775C>A	NCBI36
NG_007462.1:g.2447C>A
NG_012010.1:g.5921C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000418386.3:c.191C>A MANE Select	ENSP00000413450.2:p.Ala64Asp
ENST00000418386.2:c.191C>A	ENSP00000413450.2:p.Ala64Asp
ENST00000454783.5:c.191C>A	ENSP00000403495.1:p.Ala64Asp
ENST00000471842.1:n.439C>A
ENST00000489638.5:n.319C>A
NM_000595.3:c.191C>A	NP_000586.2:p.Ala64Asp
NM_001159740.2:c.191C>A	NP_001153212.1:p.Ala64Asp
XM_011514614.1:c.191C>A	XP_011512916.1:p.Ala64Asp
XM_011514615.1:c.191C>A	XP_011512917.1:p.Ala64Asp
XM_011514616.1:c.191C>A	XP_011512918.1:p.Ala64Asp
XM_011514617.1:c.191C>A	XP_011512919.1:p.Ala64Asp
XM_011514618.1:c.191C>A	XP_011512920.1:p.Ala64Asp
XM_011514615.2:c.191C>A	XP_011512917.1:p.Ala64Asp
XM_011514616.2:c.191C>A	XP_011512918.1:p.Ala64Asp
XM_011514617.2:c.191C>A	XP_011512919.1:p.Ala64Asp
NM_000595.4:c.191C>A MANE Select	NP_000586.2:p.Ala64Asp