Canonical Allele Identifier: CA2636827211

Gene: SARM1 SLC46A1

Linked Data

• gnomAD v4: 17-28399509-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399515_28399516del , CM000679.2:g.28399515_28399516del	GRCh38
NC_000017.10:g.26726531_26726532del , CM000679.1:g.26726531_26726532del	GRCh37
NC_000017.9:g.23750658_23750659del	NCBI36
NG_013306.1:g.11701_11702del , LRG_183:g.11701_11702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3229_*3230del (SARM1) MANE Select	ENSP00000468032.2:n.*3229_*3230del
ENST00000612814.5:c.*145_*146del (SLC46A1) MANE Select	ENSP00000480703.1:n.*145_*146del
ENST00000582735.1:c.409_410del (SLC46A1)
ENST00000585482.5:c.*3229_*3230del (SARM1)	ENSP00000468032.2:n.*3229_*3230del
ENST00000612814.4:c.*145_*146del (SLC46A1)	ENSP00000480703.1:n.*145_*146del
ENST00000618626.1:c.*145_*146del (SLC46A1)	ENSP00000483652.1:n.*145_*146del
NM_001242366.2:c.*145_*146del (SLC46A1)	NP_001229295.1:n.*145_*146del
NM_015077.3:c.*3229_*3230del (SARM1)	NP_055892.2:n.*3229_*3230del
NM_080669.5:c.*145_*146del (SLC46A1)	NP_542400.2:n.*145_*146del
XM_005277786.2:c.*36_*37del (SLC46A1)	XP_005277843.1:n.*36_*37del
XM_005277786.3:c.*36_*37del (SLC46A1)	XP_005277843.1:n.*36_*37del
XM_017024110.1:c.*145_*146del (SLC46A1)	XP_016879599.1:n.*145_*146del
NM_015077.4:c.*3229_*3230del (SARM1) MANE Select	NP_055892.2:n.*3229_*3230del
NM_080669.6:c.*145_*146del (SLC46A1) MANE Select	NP_542400.2:n.*145_*146del
NM_001242366.3:c.*145_*146del (SLC46A1)	NP_001229295.1:n.*145_*146del