Canonical Allele Identifier: CA499092429

Gene: SARM1 SLC46A1

Linked Data

• MyVariant Identifiers: chr17:g.26726708A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399692A>T , CM000679.2:g.28399692A>T	GRCh38
NC_000017.10:g.26726708A>T , CM000679.1:g.26726708A>T	GRCh37
NC_000017.9:g.23750835A>T	NCBI36
NG_013306.1:g.11520T>A , LRG_183:g.11520T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3406A>T (SARM1) MANE Select	ENSP00000468032.2:n.*3406A>T
ENST00000612814.5:c.1344T>A (SLC46A1) MANE Select	ENSP00000480703.1:p.Pro448=
ENST00000582735.1:c.228T>A (SLC46A1)
ENST00000585482.5:c.*3406A>T (SARM1)	ENSP00000468032.2:n.*3406A>T
ENST00000612814.4:c.1344T>A (SLC46A1)	ENSP00000480703.1:p.Pro448=
ENST00000618626.1:c.1260T>A (SLC46A1)	ENSP00000483652.1:p.Pro420=
NM_001242366.2:c.1260T>A (SLC46A1)	NP_001229295.1:p.Pro420=
NM_015077.3:c.*3406A>T (SARM1)	NP_055892.2:n.*3406A>T
NM_080669.5:c.1344T>A (SLC46A1)	NP_542400.2:p.Pro448=
XM_005277786.2:c.1103T>A (SLC46A1)	XP_005277843.1:p.Leu368His
XM_005277786.3:c.1103T>A (SLC46A1)	XP_005277843.1:p.Leu368His
XM_017024110.1:c.1122T>A (SLC46A1)	XP_016879599.1:p.Pro374=
NM_015077.4:c.*3406A>T (SARM1) MANE Select	NP_055892.2:n.*3406A>T
NM_080669.6:c.1344T>A (SLC46A1) MANE Select	NP_542400.2:p.Pro448=
NM_001242366.3:c.1260T>A (SLC46A1)	NP_001229295.1:p.Pro420=