Canonical Allele Identifier: CA499093791
Gene: SARM1 HGNC NCBI
SLC46A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.26729351C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28402333C>G , CM000679.2:g.28402333C>G GRCh38
NC_000017.10:g.26729351C>G , CM000679.1:g.26729351C>G GRCh37
NC_000017.9:g.23753478C>G NCBI36
NG_013306.1:g.8878G>C , LRG_183:g.8878G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000585482.6:c.*6047C>G (SARM1) MANE Select ENSP00000468032.2:n.*6047C>G
ENST00000612814.5:c.1082-12G>C (SLC46A1) MANE Select ENSP00000480703.1:n.1082-12G>C
ENST00000582735.1:c.206+2283G>C (SLC46A1)
ENST00000585482.5:c.*6047C>G (SARM1) ENSP00000468032.2:n.*6047C>G
ENST00000612814.4:c.1082-12G>C (SLC46A1) ENSP00000480703.1:n.1082-12G>C
ENST00000618626.1:c.1082-1567G>C (SLC46A1) ENSP00000483652.1:n.1082-1567G>C
NM_001242366.2:c.1082-1567G>C (SLC46A1) NP_001229295.1:n.1082-1567G>C
NM_080669.5:c.1082-12G>C (SLC46A1) NP_542400.2:n.1082-12G>C
XM_005277786.2:c.1081+2283G>C (SLC46A1) XP_005277843.1:n.1081+2283G>C
XM_005277786.3:c.1081+2283G>C (SLC46A1) XP_005277843.1:n.1081+2283G>C
XM_017024110.1:c.860-12G>C (SLC46A1) XP_016879599.1:n.860-12G>C
NM_015077.4:c.*6047C>G (SARM1) MANE Select NP_055892.2:n.*6047C>G
NM_080669.6:c.1082-12G>C (SLC46A1) MANE Select NP_542400.2:n.1082-12G>C
NM_001242366.3:c.1082-1567G>C (SLC46A1) NP_001229295.1:n.1082-1567G>C