Canonical Allele Identifier: CA727736064

Gene: SARM1 SLC46A1

Linked Data

• dbSNP Id: rs1346730075
• MyVariant Identifiers: chr17:g.28399654G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.28399654G>C , CM000679.2:g.28399654G>C	GRCh38
NC_000017.10:g.26726670G>C , CM000679.1:g.26726670G>C	GRCh37
NC_000017.9:g.23750797G>C	NCBI36
NG_013306.1:g.11558C>G , LRG_183:g.11558C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585482.6:c.*3368G>C (SARM1) MANE Select	ENSP00000468032.2:n.*3368G>C
ENST00000612814.5:c.*2C>G (SLC46A1) MANE Select	ENSP00000480703.1:n.*2C>G
ENST00000582735.1:c.266C>G (SLC46A1)
ENST00000585482.5:c.*3368G>C (SARM1)	ENSP00000468032.2:n.*3368G>C
ENST00000612814.4:c.*2C>G (SLC46A1)	ENSP00000480703.1:n.*2C>G
ENST00000618626.1:c.*2C>G (SLC46A1)	ENSP00000483652.1:n.*2C>G
NM_001242366.2:c.*2C>G (SLC46A1)	NP_001229295.1:n.*2C>G
NM_015077.3:c.*3368G>C (SARM1)	NP_055892.2:n.*3368G>C
NM_080669.5:c.*2C>G (SLC46A1)	NP_542400.2:n.*2C>G
XM_005277786.2:c.1141C>G (SLC46A1)	XP_005277843.1:p.Leu381Val
XM_005277786.3:c.1141C>G (SLC46A1)	XP_005277843.1:p.Leu381Val
XM_017024110.1:c.*2C>G (SLC46A1)	XP_016879599.1:n.*2C>G
NM_015077.4:c.*3368G>C (SARM1) MANE Select	NP_055892.2:n.*3368G>C
NM_080669.6:c.*2C>G (SLC46A1) MANE Select	NP_542400.2:n.*2C>G
NM_001242366.3:c.*2C>G (SLC46A1)	NP_001229295.1:n.*2C>G