Canonical Allele Identifier: CA385671913
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239976A>G , CM000674.2:g.65239976A>G GRCh38
NC_000012.11:g.65633756A>G , CM000674.1:g.65633756A>G GRCh37
NC_000012.10:g.63920023A>G NCBI36
NG_016210.1:g.75406A>G
NG_016210.2:g.75406A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1969A>G MANE Select ENSP00000308369.2:p.Thr657Ala
ENST00000308330.2:c.1969A>G ENSP00000308369.2:p.Thr657Ala
NM_001167614.1:c.1966A>G NP_001161086.1:p.Thr656Ala
NM_014319.4:c.1969A>G NP_055134.2:p.Thr657Ala
NM_014319.5:c.1969A>G MANE Select NP_055134.2:p.Thr657Ala
NM_001167614.2:c.1966A>G NP_001161086.1:p.Thr656Ala