Canonical Allele Identifier: CA2254286581

Gene: SARM1 SLC46A1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399515C= , CM000679.2:g.28399515C=	GRCh38
NC_000017.10:g.26726531C= , CM000679.1:g.26726531C=	GRCh37
NC_000017.9:g.23750658C=	NCBI36
NG_013306.1:g.11697G= , LRG_183:g.11697G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3229C= (SARM1) MANE Select	ENSP00000468032.2:n.*3229C=
ENST00000612814.5:c.*141G= (SLC46A1) MANE Select	ENSP00000480703.1:n.*141G=
ENST00000582735.1:c.405G= (SLC46A1)
ENST00000585482.5:c.*3229C= (SARM1)	ENSP00000468032.2:n.*3229C=
ENST00000612814.4:c.*141G= (SLC46A1)	ENSP00000480703.1:n.*141G=
ENST00000618626.1:c.*141G= (SLC46A1)	ENSP00000483652.1:n.*141G=
NM_001242366.2:c.*141G= (SLC46A1)	NP_001229295.1:n.*141G=
NM_015077.3:c.*3229C= (SARM1)	NP_055892.2:n.*3229C=
NM_080669.5:c.*141G= (SLC46A1)	NP_542400.2:n.*141G=
XM_005277786.2:c.*32G= (SLC46A1)	XP_005277843.1:n.*32G=
XM_005277786.3:c.*32G= (SLC46A1)	XP_005277843.1:n.*32G=
XM_017024110.1:c.*141G= (SLC46A1)	XP_016879599.1:n.*141G=
NM_015077.4:c.*3229C= (SARM1) MANE Select	NP_055892.2:n.*3229C=
NM_080669.6:c.*141G= (SLC46A1) MANE Select	NP_542400.2:n.*141G=
NM_001242366.3:c.*141G= (SLC46A1)	NP_001229295.1:n.*141G=