Canonical Allele Identifier: CA2636827307

Gene: SARM1 SLC46A1

Linked Data

• gnomAD v4: 17-28399714-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399715del , CM000679.2:g.28399715del	GRCh38
NC_000017.10:g.26726731del , CM000679.1:g.26726731del	GRCh37
NC_000017.9:g.23750858del	NCBI36
NG_013306.1:g.11497del , LRG_183:g.11497del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3429del (SARM1) MANE Select	ENSP00000468032.2:n.*3429del
ENST00000612814.5:c.1323-2del (SLC46A1) MANE Select	ENSP00000480703.1:n.1323-2del
ENST00000582735.1:c.207-2del (SLC46A1)
ENST00000585482.5:c.*3429del (SARM1)	ENSP00000468032.2:n.*3429del
ENST00000612814.4:c.1323-2del (SLC46A1)	ENSP00000480703.1:n.1323-2del
ENST00000618626.1:c.1239-2del (SLC46A1)	ENSP00000483652.1:n.1239-2del
NM_001242366.2:c.1239-2del (SLC46A1)	NP_001229295.1:n.1239-2del
NM_015077.3:c.*3429del (SARM1)	NP_055892.2:n.*3429del
NM_080669.5:c.1323-2del (SLC46A1)	NP_542400.2:n.1323-2del
XM_005277786.2:c.1082-2del (SLC46A1)	XP_005277843.1:n.1082-2del
XM_005277786.3:c.1082-2del (SLC46A1)	XP_005277843.1:n.1082-2del
XM_017024110.1:c.1101-2del (SLC46A1)	XP_016879599.1:n.1101-2del
NM_015077.4:c.*3429del (SARM1) MANE Select	NP_055892.2:n.*3429del
NM_080669.6:c.1323-2del (SLC46A1) MANE Select	NP_542400.2:n.1323-2del
NM_001242366.3:c.1239-2del (SLC46A1)	NP_001229295.1:n.1239-2del