Canonical Allele Identifier: CA398340969
Gene: SARM1 HGNC NCBI
SLC46A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28399680G>T , CM000679.2:g.28399680G>T GRCh38
NC_000017.10:g.26726696G>T , CM000679.1:g.26726696G>T GRCh37
NC_000017.9:g.23750823G>T NCBI36
NG_013306.1:g.11532C>A , LRG_183:g.11532C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585482.6:c.*3394G>T (SARM1) MANE Select ENSP00000468032.2:n.*3394G>T
ENST00000612814.5:c.1356C>A (SLC46A1) MANE Select ENSP00000480703.1:p.Phe452Leu
ENST00000582735.1:c.240C>A (SLC46A1)
ENST00000585482.5:c.*3394G>T (SARM1) ENSP00000468032.2:n.*3394G>T
ENST00000612814.4:c.1356C>A (SLC46A1) ENSP00000480703.1:p.Phe452Leu
ENST00000618626.1:c.1272C>A (SLC46A1) ENSP00000483652.1:p.Phe424Leu
NM_001242366.2:c.1272C>A (SLC46A1) NP_001229295.1:p.Phe424Leu
NM_015077.3:c.*3394G>T (SARM1) NP_055892.2:n.*3394G>T
NM_080669.5:c.1356C>A (SLC46A1) NP_542400.2:p.Phe452Leu
XM_005277786.2:c.1115C>A (SLC46A1) XP_005277843.1:p.Ser372Tyr
XM_005277786.3:c.1115C>A (SLC46A1) XP_005277843.1:p.Ser372Tyr
XM_017024110.1:c.1134C>A (SLC46A1) XP_016879599.1:p.Phe378Leu
NM_015077.4:c.*3394G>T (SARM1) MANE Select NP_055892.2:n.*3394G>T
NM_080669.6:c.1356C>A (SLC46A1) MANE Select NP_542400.2:p.Phe452Leu
NM_001242366.3:c.1272C>A (SLC46A1) NP_001229295.1:p.Phe424Leu