Canonical Allele Identifier: CA2254286298
Gene: SARM1 HGNC NCBI
SLC46A1 HGNC NCBI

Linked Data

dbSNP Id: rs2239907

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28398728T>G , CM000679.2:g.28398728T>G GRCh38
NC_000017.10:g.26725744T>G , CM000679.1:g.26725744T>G GRCh37
NC_000017.9:g.23749871T>G NCBI36
NG_013306.1:g.12484A>C , LRG_183:g.12484A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000585482.6:c.*2442T>G (SARM1) MANE Select ENSP00000468032.2:n.*2442T>G
ENST00000612814.5:c.*928A>C (SLC46A1) MANE Select ENSP00000480703.1:n.*928A>C
ENST00000585482.5:c.*2442T>G (SARM1) ENSP00000468032.2:n.*2442T>G
ENST00000612814.4:c.*928A>C (SLC46A1) ENSP00000480703.1:n.*928A>C
ENST00000618626.1:c.*928A>C (SLC46A1) ENSP00000483652.1:n.*928A>C
NM_001242366.2:c.*928A>C (SLC46A1) NP_001229295.1:n.*928A>C
NM_015077.3:c.*2442T>G (SARM1) NP_055892.2:n.*2442T>G
NM_080669.5:c.*928A>C (SLC46A1) NP_542400.2:n.*928A>C
XM_005277786.2:c.*819A>C (SLC46A1) XP_005277843.1:n.*819A>C
XM_005277786.3:c.*819A>C (SLC46A1) XP_005277843.1:n.*819A>C
XM_017024110.1:c.*928A>C (SLC46A1) XP_016879599.1:n.*928A>C
NM_015077.4:c.*2442T>G (SARM1) MANE Select NP_055892.2:n.*2442T>G
NM_080669.6:c.*928A>C (SLC46A1) MANE Select NP_542400.2:n.*928A>C
NM_001242366.3:c.*928A>C (SLC46A1) NP_001229295.1:n.*928A>C