Canonical Allele Identifier: CA499092449

Gene: SARM1 SLC46A1

Linked Data

• MyVariant Identifiers: chr17:g.26726723C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399707C>A , CM000679.2:g.28399707C>A	GRCh38
NC_000017.10:g.26726723C>A , CM000679.1:g.26726723C>A	GRCh37
NC_000017.9:g.23750850C>A	NCBI36
NG_013306.1:g.11505G>T , LRG_183:g.11505G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3421C>A (SARM1) MANE Select	ENSP00000468032.2:n.*3421C>A
ENST00000612814.5:c.1329G>T (SLC46A1) MANE Select	ENSP00000480703.1:p.Leu443=
ENST00000582735.1:c.213G>T (SLC46A1)
ENST00000585482.5:c.*3421C>A (SARM1)	ENSP00000468032.2:n.*3421C>A
ENST00000612814.4:c.1329G>T (SLC46A1)	ENSP00000480703.1:p.Leu443=
ENST00000618626.1:c.1245G>T (SLC46A1)	ENSP00000483652.1:p.Leu415=
NM_001242366.2:c.1245G>T (SLC46A1)	NP_001229295.1:p.Leu415=
NM_015077.3:c.*3421C>A (SARM1)	NP_055892.2:n.*3421C>A
NM_080669.5:c.1329G>T (SLC46A1)	NP_542400.2:p.Leu443=
XM_005277786.2:c.1088G>T (SLC46A1)	XP_005277843.1:p.Trp363Leu
XM_005277786.3:c.1088G>T (SLC46A1)	XP_005277843.1:p.Trp363Leu
XM_017024110.1:c.1107G>T (SLC46A1)	XP_016879599.1:p.Leu369=
NM_015077.4:c.*3421C>A (SARM1) MANE Select	NP_055892.2:n.*3421C>A
NM_080669.6:c.1329G>T (SLC46A1) MANE Select	NP_542400.2:p.Leu443=
NM_001242366.3:c.1245G>T (SLC46A1)	NP_001229295.1:p.Leu415=