Canonical Allele Identifier: CA8458357
Community Standard Title: NM_080669.6(SLC46A1):c.277G>A (p.Gly93Ser)
Gene: SLC46A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28405420C>T , CM000679.2:g.28405420C>T GRCh38
NC_000017.10:g.26732438C>T , CM000679.1:g.26732438C>T GRCh37
NC_000017.9:g.23756565C>T NCBI36
NG_013306.1:g.5791G>A , LRG_183:g.5791G>A

Transcript Alleles

HGVS Amino-acid Change
NM_080669.6:c.277G>A MANE Select NP_542400.2:p.Gly93Ser
ENST00000612814.5:c.277G>A MANE Select ENSP00000480703.1:p.Gly93Ser
NM_001242366.2:c.277G>A NP_001229295.1:p.Gly93Ser
NM_001242366.3:c.277G>A NP_001229295.1:p.Gly93Ser
NM_080669.5:c.277G>A NP_542400.2:p.Gly93Ser
ENST00000578217.1:n.67+261G>A
ENST00000581516.1:c.55G>A ENSP00000462942.1:p.Gly19Ser
ENST00000582590.1:n.331G>A
ENST00000584426.1:c.13G>A ENSP00000467416.1:p.Gly5Ser
ENST00000584995.5:c.55G>A ENSP00000464190.1:p.Gly19Ser
ENST00000612814.4:c.277G>A ENSP00000480703.1:p.Gly93Ser
ENST00000618626.1:c.277G>A ENSP00000483652.1:p.Gly93Ser
XM_005277786.2:c.277G>A XP_005277843.1:p.Gly93Ser
XM_005277786.3:c.277G>A XP_005277843.1:p.Gly93Ser
XM_017024110.1:c.55G>A XP_016879599.1:p.Gly19Ser
XR_934643.1:n.58C>T