Canonical Allele Identifier: CA2254288895

Gene: SLC46A1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28405757C= , CM000679.2:g.28405757C=	GRCh38
NC_000017.10:g.26732775C= , CM000679.1:g.26732775C=	GRCh37
NC_000017.9:g.23756902C=	NCBI36
NG_013306.1:g.5454G= , LRG_183:g.5454G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000612814.5:c.228+130G= MANE Select	ENSP00000480703.1:n.228+130G=
ENST00000581516.1:c.6+130G=	ENSP00000462942.1:n.6+130G=
ENST00000582590.1:n.282+130G=
ENST00000584426.1:c.-36-289G=	ENSP00000467416.1:n.-36-289G=
ENST00000584995.5:c.6+130G=	ENSP00000464190.1:n.6+130G=
ENST00000612814.4:c.228+130G=	ENSP00000480703.1:n.228+130G=
ENST00000618626.1:c.228+130G=	ENSP00000483652.1:n.228+130G=
NM_001242366.2:c.228+130G=	NP_001229295.1:n.228+130G=
NM_080669.5:c.228+130G=	NP_542400.2:n.228+130G=
XM_005277786.2:c.228+130G=	XP_005277843.1:n.228+130G=
XR_934643.1:n.89+306C=
XM_005277786.3:c.228+130G=	XP_005277843.1:n.228+130G=
XM_017024110.1:c.6+130G=	XP_016879599.1:n.6+130G=
NM_080669.6:c.228+130G= MANE Select	NP_542400.2:n.228+130G=
NM_001242366.3:c.228+130G=	NP_001229295.1:n.228+130G=