Canonical Allele Identifier: CA385676619
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65640010T>C (hg19) chr12:g.65246230T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246230T>C , CM000674.2:g.65246230T>C GRCh38
NC_000012.11:g.65640010T>C , CM000674.1:g.65640010T>C GRCh37
NC_000012.10:g.63926277T>C NCBI36
NG_016210.1:g.81660T>C
NG_016210.2:g.81660T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2641T>C MANE Select ENSP00000308369.2:p.Ser881Pro
ENST00000308330.2:c.2641T>C ENSP00000308369.2:p.Ser881Pro
ENST00000539442.1:n.623T>C
ENST00000544506.1:n.361T>C
ENST00000545026.1:n.459T>C
NM_001167614.1:c.2638T>C NP_001161086.1:p.Ser880Pro
NM_014319.4:c.2641T>C NP_055134.2:p.Ser881Pro
NM_014319.5:c.2641T>C MANE Select NP_055134.2:p.Ser881Pro
NM_001167614.2:c.2638T>C NP_001161086.1:p.Ser880Pro
Search 100 bp 5'
Search 100 bp 3'