Canonical Allele Identifier: CA385673554
Gene: LEMD3 HGNC NCBI

Linked Data

dbSNP Id: rs1393609335

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65170191G>T , CM000674.2:g.65170191G>T GRCh38
NC_000012.11:g.65563971G>T , CM000674.1:g.65563971G>T GRCh37
NC_000012.10:g.63850238G>T NCBI36
NG_016210.1:g.5621G>T
NG_016210.2:g.5621G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.595G>T MANE Select ENSP00000308369.2:p.Ala199Ser
ENST00000308330.2:c.595G>T ENSP00000308369.2:p.Ala199Ser
ENST00000541171.1:n.609G>T
NM_001167614.1:c.595G>T NP_001161086.1:p.Ala199Ser
NM_014319.4:c.595G>T NP_055134.2:p.Ala199Ser
NM_014319.5:c.595G>T MANE Select NP_055134.2:p.Ala199Ser
NM_001167614.2:c.595G>T NP_001161086.1:p.Ala199Ser