Canonical Allele Identifier: CA398341149

Gene: SARM1 SLC46A1

Linked Data

• MyVariant Identifiers: chr17:g.26726715G>T (hg19) ; chr17:g.28399699G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399699G>T , CM000679.2:g.28399699G>T	GRCh38
NC_000017.10:g.26726715G>T , CM000679.1:g.26726715G>T	GRCh37
NC_000017.9:g.23750842G>T	NCBI36
NG_013306.1:g.11513C>A , LRG_183:g.11513C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3413G>T (SARM1) MANE Select	ENSP00000468032.2:n.*3413G>T
ENST00000612814.5:c.1337C>A (SLC46A1) MANE Select	ENSP00000480703.1:p.Ala446Asp
ENST00000582735.1:c.221C>A (SLC46A1)
ENST00000585482.5:c.*3413G>T (SARM1)	ENSP00000468032.2:n.*3413G>T
ENST00000612814.4:c.1337C>A (SLC46A1)	ENSP00000480703.1:p.Ala446Asp
ENST00000618626.1:c.1253C>A (SLC46A1)	ENSP00000483652.1:p.Ala418Asp
NM_001242366.2:c.1253C>A (SLC46A1)	NP_001229295.1:p.Ala418Asp
NM_015077.3:c.*3413G>T (SARM1)	NP_055892.2:n.*3413G>T
NM_080669.5:c.1337C>A (SLC46A1)	NP_542400.2:p.Ala446Asp
XM_005277786.2:c.1096C>A (SLC46A1)	XP_005277843.1:p.Leu366Met
XM_005277786.3:c.1096C>A (SLC46A1)	XP_005277843.1:p.Leu366Met
XM_017024110.1:c.1115C>A (SLC46A1)	XP_016879599.1:p.Ala372Asp
NM_015077.4:c.*3413G>T (SARM1) MANE Select	NP_055892.2:n.*3413G>T
NM_080669.6:c.1337C>A (SLC46A1) MANE Select	NP_542400.2:p.Ala446Asp
NM_001242366.3:c.1253C>A (SLC46A1)	NP_001229295.1:p.Ala418Asp