Canonical Allele Identifier: CA3713789

Gene: LTA

Linked Data

• dbSNP Id: rs749181668
• ExAC: 6:31540713 T / C
• gnomAD v2: 6-31540713-T-C
• MyVariant Identifiers: chr6:g.31540713T>C (hg19) ; chr6:g.31572936T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31572936T>C , CM000668.2:g.31572936T>C	GRCh38
NC_000006.11:g.31540713T>C , CM000668.1:g.31540713T>C	GRCh37
NC_000006.10:g.31648692T>C	NCBI36
NG_007462.1:g.2364T>C
NG_012010.1:g.5838T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000418386.3:c.108T>C MANE Select	ENSP00000413450.2:p.Pro36=
ENST00000418386.2:c.108T>C	ENSP00000413450.2:p.Pro36=
ENST00000454783.5:c.108T>C	ENSP00000403495.1:p.Pro36=
ENST00000471842.1:n.356T>C
ENST00000489638.5:n.236T>C
NM_000595.3:c.108T>C	NP_000586.2:p.Pro36=
NM_001159740.2:c.108T>C	NP_001153212.1:p.Pro36=
XM_011514614.1:c.108T>C	XP_011512916.1:p.Pro36=
XM_011514615.1:c.108T>C	XP_011512917.1:p.Pro36=
XM_011514616.1:c.108T>C	XP_011512918.1:p.Pro36=
XM_011514617.1:c.108T>C	XP_011512919.1:p.Pro36=
XM_011514618.1:c.108T>C	XP_011512920.1:p.Pro36=
XM_011514615.2:c.108T>C	XP_011512917.1:p.Pro36=
XM_011514616.2:c.108T>C	XP_011512918.1:p.Pro36=
XM_011514617.2:c.108T>C	XP_011512919.1:p.Pro36=
NM_000595.4:c.108T>C MANE Select	NP_000586.2:p.Pro36=