Canonical Allele Identifier: CA480666138

Gene: LEMD3

Linked Data

• MyVariant Identifiers: chr12:g.65632503T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65238723T>C , CM000674.2:g.65238723T>C	GRCh38
NC_000012.11:g.65632503T>C , CM000674.1:g.65632503T>C	GRCh37
NC_000012.10:g.63918770T>C	NCBI36
NG_016210.1:g.74153T>C
NG_016210.2:g.74153T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.1830T>C MANE Select	ENSP00000308369.2:p.Phe610=
ENST00000308330.2:c.1830T>C	ENSP00000308369.2:p.Phe610=
NM_001167614.1:c.1827T>C	NP_001161086.1:p.Phe609=
NM_014319.4:c.1830T>C	NP_055134.2:p.Phe610=
NM_014319.5:c.1830T>C MANE Select	NP_055134.2:p.Phe610=
NM_001167614.2:c.1827T>C	NP_001161086.1:p.Phe609=