Canonical Allele Identifier: CA374774941
Gene: LHX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.122228720G>T , CM000671.2:g.122228720G>T GRCh38
NC_000009.11:g.124990999G>T , CM000671.1:g.124990999G>T GRCh37
NC_000009.10:g.124030820G>T NCBI36
NG_029683.1:g.5093C>A

Transcript Alleles

HGVS Amino-acid Change
NM_014368.5:c.21C>A MANE Select NP_055183.2:p.Asn7Lys
ENST00000394319.9:c.21C>A MANE Select ENSP00000377854.4:p.Asn7Lys
NM_014368.4:c.21C>A NP_055183.2:p.Asn7Lys
NM_199160.3:c.21C>A NP_954629.2:p.Asn7Lys
NM_199160.4:c.21C>A NP_954629.2:p.Asn7Lys
ENST00000340587.7:c.21C>A ENSP00000340137.3:p.Asn7Lys
ENST00000394319.8:c.21C>A ENSP00000377854.4:p.Asn7Lys
ENST00000559529.1:n.362C>A
XM_005251916.3:c.21C>A XP_005251973.1:p.Asn7Lys
XM_011518521.1:c.21C>A XP_011516823.1:p.Asn7Lys
XM_011518521.2:c.21C>A XP_011516823.1:p.Asn7Lys
XM_011518523.1:c.21C>A XP_011516825.1:p.Asn7Lys