Canonical Allele Identifier: CA383035841
Gene: SORL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121558673G>C , CM000673.2:g.121558673G>C GRCh38
NC_000011.9:g.121429382G>C , CM000673.1:g.121429382G>C GRCh37
NC_000011.8:g.120934592G>C NCBI36
NG_023313.1:g.111422G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.2746G>C MANE Select ENSP00000260197.6:p.Val916Leu
ENST00000260197.11:c.2746G>C ENSP00000260197.6:p.Val916Leu
ENST00000524873.1:n.474G>C
ENST00000529445.1:n.452G>C
NM_003105.5:c.2746G>C NP_003096.1:p.Val916Leu
XM_011542963.1:c.2746G>C XP_011541265.1:p.Val916Leu
XM_011542964.1:c.2746G>C XP_011541266.1:p.Val916Leu
XM_011542965.1:c.1207G>C XP_011541267.1:p.Val403Leu
XM_011542966.1:c.106G>C XP_011541268.1:p.Val36Leu
XM_011542963.3:c.2746G>C XP_011541265.1:p.Val916Leu
XM_011542965.3:c.1207G>C XP_011541267.1:p.Val403Leu
XM_017018169.2:c.2434G>C XP_016873658.1:p.Val812Leu
XM_017018170.2:c.2221G>C XP_016873659.1:p.Val741Leu
XM_017018171.1:c.2746G>C XP_016873660.1:p.Val916Leu
XM_017018172.2:c.106G>C XP_016873661.1:p.Val36Leu
NM_003105.6:c.2746G>C MANE Select NP_003096.2:p.Val916Leu