Canonical Allele Identifier: CA2254287689

Gene: SARM1 SLC46A1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28402277G= , CM000679.2:g.28402277G=	GRCh38
NC_000017.10:g.26729295G= , CM000679.1:g.26729295G=	GRCh37
NC_000017.9:g.23753422G=	NCBI36
NG_013306.1:g.8934C= , LRG_183:g.8934C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*5991G= (SARM1) MANE Select	ENSP00000468032.2:n.*5991G=
ENST00000612814.5:c.1126C= (SLC46A1) MANE Select	ENSP00000480703.1:p.Arg376=
ENST00000582735.1:c.206+2339C= (SLC46A1)
ENST00000585482.5:c.*5991G= (SARM1)	ENSP00000468032.2:n.*5991G=
ENST00000612814.4:c.1126C= (SLC46A1)	ENSP00000480703.1:p.Arg376=
ENST00000618626.1:c.1082-1511C= (SLC46A1)	ENSP00000483652.1:n.1082-1511C=
NM_001242366.2:c.1082-1511C= (SLC46A1)	NP_001229295.1:n.1082-1511C=
NM_080669.5:c.1126C= (SLC46A1)	NP_542400.2:p.Arg376=
XM_005277786.2:c.1081+2339C= (SLC46A1)	XP_005277843.1:n.1081+2339C=
XM_005277786.3:c.1081+2339C= (SLC46A1)	XP_005277843.1:n.1081+2339C=
XM_017024110.1:c.904C= (SLC46A1)	XP_016879599.1:p.Arg302=
NM_015077.4:c.*5991G= (SARM1) MANE Select	NP_055892.2:n.*5991G=
NM_080669.6:c.1126C= (SLC46A1) MANE Select	NP_542400.2:p.Arg376=
NM_001242366.3:c.1082-1511C= (SLC46A1)	NP_001229295.1:n.1082-1511C=