Canonical Allele Identifier: CA2505507803
Gene: SARM1 HGNC NCBI
SLC46A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28402337_28402351del , CM000679.2:g.28402337_28402351del GRCh38
NC_000017.10:g.26729355_26729369del , CM000679.1:g.26729355_26729369del GRCh37
NC_000017.9:g.23753482_23753496del NCBI36
NG_013306.1:g.8863_8877del , LRG_183:g.8863_8877del

Transcript Alleles

HGVS Amino-acid change
ENST00000585482.6:c.*6051_*6065del (SARM1) MANE Select ENSP00000468032.2:n.*6051_*6065del
ENST00000612814.5:c.1082-27_1082-13del (SLC46A1) MANE Select ENSP00000480703.1:n.1082-27_1082-13del
ENST00000582735.1:c.206+2268_206+2282del (SLC46A1)
ENST00000585482.5:c.*6051_*6065del (SARM1) ENSP00000468032.2:n.*6051_*6065del
ENST00000612814.4:c.1082-27_1082-13del (SLC46A1) ENSP00000480703.1:n.1082-27_1082-13del
ENST00000618626.1:c.1082-1582_1082-1568del (SLC46A1) ENSP00000483652.1:n.1082-1582_1082-1568del
NM_001242366.2:c.1082-1582_1082-1568del (SLC46A1) NP_001229295.1:n.1082-1582_1082-1568del
NM_080669.5:c.1082-27_1082-13del (SLC46A1) NP_542400.2:n.1082-27_1082-13del
XM_005277786.2:c.1081+2268_1081+2282del (SLC46A1) XP_005277843.1:n.1081+2268_1081+2282del
XM_005277786.3:c.1081+2268_1081+2282del (SLC46A1) XP_005277843.1:n.1081+2268_1081+2282del
XM_017024110.1:c.860-27_860-13del (SLC46A1) XP_016879599.1:n.860-27_860-13del
NM_015077.4:c.*6051_*6065del (SARM1) MANE Select NP_055892.2:n.*6051_*6065del
NM_080669.6:c.1082-27_1082-13del (SLC46A1) MANE Select NP_542400.2:n.1082-27_1082-13del
NM_001242366.3:c.1082-1582_1082-1568del (SLC46A1) NP_001229295.1:n.1082-1582_1082-1568del