Canonical Allele Identifier: CA291912
Community Standard Title: NM_003240.5(LEFTY2):c.497+13C>G
Gene: LEFTY2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.225939743G>C , CM000663.2:g.225939743G>C GRCh38
NC_000001.10:g.226127443G>C , CM000663.1:g.226127443G>C GRCh37
NC_000001.9:g.224194066G>C NCBI36
NG_008118.1:g.6478C>G

Transcript Alleles

HGVS Amino-acid Change
NM_003240.5:c.497+13C>G MANE Select NP_003231.2:n.497+13C>G
ENST00000366820.10:c.497+13C>G MANE Select ENSP00000355785.5:n.497+13C>G
NM_001172425.1:c.395+13C>G NP_001165896.1:n.395+13C>G
NM_001172425.2:c.395+13C>G NP_001165896.1:n.395+13C>G
NM_001172425.3:c.395+13C>G NP_001165896.1:n.395+13C>G
NM_003240.3:c.497+13C>G NP_003231.2:n.497+13C>G
NM_003240.4:c.497+13C>G NP_003231.2:n.497+13C>G
ENST00000366820.9:c.497+13C>G ENSP00000355785.5:n.497+13C>G
ENST00000420304.6:c.395+13C>G ENSP00000388009.2:n.395+13C>G
ENST00000474493.1:n.346+13C>G
ENST00000616737.1:c.497+13C>G ENSP00000484300.1:n.497+13C>G
XM_011544266.1:c.497+13C>G XP_011542568.1:n.497+13C>G