Canonical Allele Identifier: CA8458326
Community Standard Title: NM_080669.6(SLC46A1):c.462C>T (p.Leu154=)
Gene: SLC46A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28405235G>A , CM000679.2:g.28405235G>A GRCh38
NC_000017.10:g.26732253G>A , CM000679.1:g.26732253G>A GRCh37
NC_000017.9:g.23756380G>A NCBI36
NG_013306.1:g.5976C>T , LRG_183:g.5976C>T

Transcript Alleles

HGVS Amino-acid Change
NM_080669.6:c.462C>T MANE Select NP_542400.2:p.Leu154=
ENST00000612814.5:c.462C>T MANE Select ENSP00000480703.1:p.Leu154=
NM_001242366.2:c.462C>T NP_001229295.1:p.Leu154=
NM_001242366.3:c.462C>T NP_001229295.1:p.Leu154=
NM_080669.5:c.462C>T NP_542400.2:p.Leu154=
ENST00000578217.1:n.67+446C>T
ENST00000582590.1:n.516C>T
ENST00000584426.1:c.198C>T ENSP00000467416.1:p.Leu66=
ENST00000584995.5:c.240C>T ENSP00000464190.1:p.Leu80=
ENST00000612814.4:c.462C>T ENSP00000480703.1:p.Leu154=
ENST00000618626.1:c.462C>T ENSP00000483652.1:p.Leu154=
XM_005277786.2:c.462C>T XP_005277843.1:p.Leu154=
XM_005277786.3:c.462C>T XP_005277843.1:p.Leu154=
XM_017024110.1:c.240C>T XP_016879599.1:p.Leu80=