Canonical Allele Identifier: CA363339276

Gene: LTA

Linked Data

• gnomAD v4: 6-31573019-C-T
• MyVariant Identifiers: chr6:g.31540796C>T (hg19) ; chr6:g.31573019C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000418386.3:c.191C>T MANE Select	ENSP00000413450.2:p.Ala64Val
ENST00000418386.2:c.191C>T	ENSP00000413450.2:p.Ala64Val
ENST00000454783.5:c.191C>T	ENSP00000403495.1:p.Ala64Val
ENST00000471842.1:n.439C>T
ENST00000489638.5:n.319C>T
NM_000595.3:c.191C>T	NP_000586.2:p.Ala64Val
NM_001159740.2:c.191C>T	NP_001153212.1:p.Ala64Val
XM_011514614.1:c.191C>T	XP_011512916.1:p.Ala64Val
XM_011514615.1:c.191C>T	XP_011512917.1:p.Ala64Val
XM_011514616.1:c.191C>T	XP_011512918.1:p.Ala64Val
XM_011514617.1:c.191C>T	XP_011512919.1:p.Ala64Val
XM_011514618.1:c.191C>T	XP_011512920.1:p.Ala64Val
XM_011514615.2:c.191C>T	XP_011512917.1:p.Ala64Val
XM_011514616.2:c.191C>T	XP_011512918.1:p.Ala64Val
XM_011514617.2:c.191C>T	XP_011512919.1:p.Ala64Val
NM_000595.4:c.191C>T MANE Select	NP_000586.2:p.Ala64Val