Canonical Allele Identifier: CA398341281
Gene: SARM1 HGNC NCBI
SLC46A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28399712T>C , CM000679.2:g.28399712T>C GRCh38
NC_000017.10:g.26726728T>C , CM000679.1:g.26726728T>C GRCh37
NC_000017.9:g.23750855T>C NCBI36
NG_013306.1:g.11500A>G , LRG_183:g.11500A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000585482.6:c.*3426T>C (SARM1) MANE Select ENSP00000468032.2:n.*3426T>C
ENST00000612814.5:c.1324A>G (SLC46A1) MANE Select ENSP00000480703.1:p.Met442Val
ENST00000582735.1:c.208A>G (SLC46A1)
ENST00000585482.5:c.*3426T>C (SARM1) ENSP00000468032.2:n.*3426T>C
ENST00000612814.4:c.1324A>G (SLC46A1) ENSP00000480703.1:p.Met442Val
ENST00000618626.1:c.1240A>G (SLC46A1) ENSP00000483652.1:p.Met414Val
NM_001242366.2:c.1240A>G (SLC46A1) NP_001229295.1:p.Met414Val
NM_015077.3:c.*3426T>C (SARM1) NP_055892.2:n.*3426T>C
NM_080669.5:c.1324A>G (SLC46A1) NP_542400.2:p.Met442Val
XM_005277786.2:c.1083A>G (SLC46A1) XP_005277843.1:p.Gly361=
XM_005277786.3:c.1083A>G (SLC46A1) XP_005277843.1:p.Gly361=
XM_017024110.1:c.1102A>G (SLC46A1) XP_016879599.1:p.Met368Val
NM_015077.4:c.*3426T>C (SARM1) MANE Select NP_055892.2:n.*3426T>C
NM_080669.6:c.1324A>G (SLC46A1) MANE Select NP_542400.2:p.Met442Val
NM_001242366.3:c.1240A>G (SLC46A1) NP_001229295.1:p.Met414Val