Canonical Allele Identifier: CA691027627

Gene: LEMD3

Linked Data

• dbSNP Id: rs1402356398
• MyVariant Identifiers: chr12:g.65632090A>T (hg19) ; chr12:g.65238310A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65238310A>T , CM000674.2:g.65238310A>T	GRCh38
NC_000012.11:g.65632090A>T , CM000674.1:g.65632090A>T	GRCh37
NC_000012.10:g.63918357A>T	NCBI36
NG_016210.1:g.73740A>T
NG_016210.2:g.73740A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.1696-192A>T MANE Select	ENSP00000308369.2:n.1696-192A>T
ENST00000308330.2:c.1696-192A>T	ENSP00000308369.2:n.1696-192A>T
NM_001167614.1:c.1693-192A>T	NP_001161086.1:n.1693-192A>T
NM_014319.4:c.1696-192A>T	NP_055134.2:n.1696-192A>T
NM_014319.5:c.1696-192A>T MANE Select	NP_055134.2:n.1696-192A>T
NM_001167614.2:c.1693-192A>T	NP_001161086.1:n.1693-192A>T