Canonical Allele Identifier: CA398340997

Gene: SARM1 SLC46A1

Linked Data

• MyVariant Identifiers: chr17:g.26726698A>G (hg19) ; chr17:g.28399682A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399682A>G , CM000679.2:g.28399682A>G	GRCh38
NC_000017.10:g.26726698A>G , CM000679.1:g.26726698A>G	GRCh37
NC_000017.9:g.23750825A>G	NCBI36
NG_013306.1:g.11530T>C , LRG_183:g.11530T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3396A>G (SARM1) MANE Select	ENSP00000468032.2:n.*3396A>G
ENST00000612814.5:c.1354T>C (SLC46A1) MANE Select	ENSP00000480703.1:p.Phe452Leu
ENST00000582735.1:c.238T>C (SLC46A1)
ENST00000585482.5:c.*3396A>G (SARM1)	ENSP00000468032.2:n.*3396A>G
ENST00000612814.4:c.1354T>C (SLC46A1)	ENSP00000480703.1:p.Phe452Leu
ENST00000618626.1:c.1270T>C (SLC46A1)	ENSP00000483652.1:p.Phe424Leu
NM_001242366.2:c.1270T>C (SLC46A1)	NP_001229295.1:p.Phe424Leu
NM_015077.3:c.*3396A>G (SARM1)	NP_055892.2:n.*3396A>G
NM_080669.5:c.1354T>C (SLC46A1)	NP_542400.2:p.Phe452Leu
XM_005277786.2:c.1113T>C (SLC46A1)	XP_005277843.1:p.Ser371=
XM_005277786.3:c.1113T>C (SLC46A1)	XP_005277843.1:p.Ser371=
XM_017024110.1:c.1132T>C (SLC46A1)	XP_016879599.1:p.Phe378Leu
NM_015077.4:c.*3396A>G (SARM1) MANE Select	NP_055892.2:n.*3396A>G
NM_080669.6:c.1354T>C (SLC46A1) MANE Select	NP_542400.2:p.Phe452Leu
NM_001242366.3:c.1270T>C (SLC46A1)	NP_001229295.1:p.Phe424Leu