Canonical Allele Identifier: CA499092435

Gene: SARM1 SLC46A1

Linked Data

• gnomAD v4: 17-28399698-A-G
• MyVariant Identifiers: chr17:g.26726714A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399698A>G , CM000679.2:g.28399698A>G	GRCh38
NC_000017.10:g.26726714A>G , CM000679.1:g.26726714A>G	GRCh37
NC_000017.9:g.23750841A>G	NCBI36
NG_013306.1:g.11514T>C , LRG_183:g.11514T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3412A>G (SARM1) MANE Select	ENSP00000468032.2:n.*3412A>G
ENST00000612814.5:c.1338T>C (SLC46A1) MANE Select	ENSP00000480703.1:p.Ala446=
ENST00000582735.1:c.222T>C (SLC46A1)
ENST00000585482.5:c.*3412A>G (SARM1)	ENSP00000468032.2:n.*3412A>G
ENST00000612814.4:c.1338T>C (SLC46A1)	ENSP00000480703.1:p.Ala446=
ENST00000618626.1:c.1254T>C (SLC46A1)	ENSP00000483652.1:p.Ala418=
NM_001242366.2:c.1254T>C (SLC46A1)	NP_001229295.1:p.Ala418=
NM_015077.3:c.*3412A>G (SARM1)	NP_055892.2:n.*3412A>G
NM_080669.5:c.1338T>C (SLC46A1)	NP_542400.2:p.Ala446=
XM_005277786.2:c.1097T>C (SLC46A1)	XP_005277843.1:p.Leu366Pro
XM_005277786.3:c.1097T>C (SLC46A1)	XP_005277843.1:p.Leu366Pro
XM_017024110.1:c.1116T>C (SLC46A1)	XP_016879599.1:p.Ala372=
NM_015077.4:c.*3412A>G (SARM1) MANE Select	NP_055892.2:n.*3412A>G
NM_080669.6:c.1338T>C (SLC46A1) MANE Select	NP_542400.2:p.Ala446=
NM_001242366.3:c.1254T>C (SLC46A1)	NP_001229295.1:p.Ala418=