Canonical Allele Identifier: CA499093779

Gene: SARM1 SLC46A1

Linked Data

• MyVariant Identifiers: chr17:g.26729349A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28402331A>C , CM000679.2:g.28402331A>C	GRCh38
NC_000017.10:g.26729349A>C , CM000679.1:g.26729349A>C	GRCh37
NC_000017.9:g.23753476A>C	NCBI36
NG_013306.1:g.8880T>G , LRG_183:g.8880T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585482.6:c.*6045A>C (SARM1) MANE Select	ENSP00000468032.2:n.*6045A>C
ENST00000612814.5:c.1082-10T>G (SLC46A1) MANE Select	ENSP00000480703.1:n.1082-10T>G
ENST00000582735.1:c.206+2285T>G (SLC46A1)
ENST00000585482.5:c.*6045A>C (SARM1)	ENSP00000468032.2:n.*6045A>C
ENST00000612814.4:c.1082-10T>G (SLC46A1)	ENSP00000480703.1:n.1082-10T>G
ENST00000618626.1:c.1082-1565T>G (SLC46A1)	ENSP00000483652.1:n.1082-1565T>G
NM_001242366.2:c.1082-1565T>G (SLC46A1)	NP_001229295.1:n.1082-1565T>G
NM_080669.5:c.1082-10T>G (SLC46A1)	NP_542400.2:n.1082-10T>G
XM_005277786.2:c.1081+2285T>G (SLC46A1)	XP_005277843.1:n.1081+2285T>G
XM_005277786.3:c.1081+2285T>G (SLC46A1)	XP_005277843.1:n.1081+2285T>G
XM_017024110.1:c.860-10T>G (SLC46A1)	XP_016879599.1:n.860-10T>G
NM_015077.4:c.*6045A>C (SARM1) MANE Select	NP_055892.2:n.*6045A>C
NM_080669.6:c.1082-10T>G (SLC46A1) MANE Select	NP_542400.2:n.1082-10T>G
NM_001242366.3:c.1082-1565T>G (SLC46A1)	NP_001229295.1:n.1082-1565T>G