Canonical Allele Identifier: CA1420421
Gene: LEFTY2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418283
dbSNP Id: rs777139964

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225937512G>T , CM000663.2:g.225937512G>T GRCh38
NC_000001.10:g.226125212G>T , CM000663.1:g.226125212G>T GRCh37
NC_000001.9:g.224191835G>T NCBI36
NG_008118.1:g.8709C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366820.10:c.1030C>A MANE Select ENSP00000355785.5:p.Pro344Thr
ENST00000366820.9:c.1030C>A ENSP00000355785.5:p.Pro344Thr
ENST00000420304.6:c.928C>A ENSP00000388009.2:p.Pro310Thr
ENST00000616737.1:c.1030C>A ENSP00000484300.1:p.Pro344Thr
NM_001172425.1:c.928C>A NP_001165896.1:p.Pro310Thr
NM_003240.3:c.1030C>A NP_003231.2:p.Pro344Thr
NM_001172425.2:c.928C>A NP_001165896.1:p.Pro310Thr
NM_003240.4:c.1030C>A NP_003231.2:p.Pro344Thr
NM_003240.5:c.1030C>A MANE Select NP_003231.2:p.Pro344Thr
NM_001172425.3:c.928C>A NP_001165896.1:p.Pro310Thr