Canonical Allele Identifier: CA2004925775
Gene: SORL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121610719G= , CM000673.2:g.121610719G= GRCh38
NC_000011.9:g.121481428G= , CM000673.1:g.121481428G= GRCh37
NC_000011.8:g.120986638G= NCBI36
NG_023313.1:g.163468G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260197.12:c.5240-357G= MANE Select ENSP00000260197.6:n.5240-357G=
ENST00000260197.11:c.5240-357G= ENSP00000260197.6:n.5240-357G=
ENST00000525532.5:c.2072-357G= ENSP00000434634.1:n.2072-357G=
ENST00000527934.1:c.1085-357G= ENSP00000435405.1:n.1085-357G=
ENST00000528339.5:n.2520G=
ENST00000532694.5:c.1778-357G= ENSP00000432131.1:n.1778-357G=
ENST00000534286.5:c.1970-357G= ENSP00000436447.1:n.1970-357G=
NM_003105.5:c.5240-357G= NP_003096.1:n.5240-357G=
XM_011542963.1:c.5126-357G= XP_011541265.1:n.5126-357G=
XM_011542964.1:c.*48-357G= XP_011541266.1:n.*48-357G=
XM_011542965.1:c.3701-357G= XP_011541267.1:n.3701-357G=
XM_011542966.1:c.2600-357G= XP_011541268.1:n.2600-357G=
XM_011542967.1:c.2072-357G= XP_011541269.1:n.2072-357G=
XM_011542963.3:c.5126-357G= XP_011541265.1:n.5126-357G=
XM_011542965.3:c.3701-357G= XP_011541267.1:n.3701-357G=
XM_011542967.3:c.2072-357G= XP_011541269.1:n.2072-357G=
XM_017018169.2:c.4928-357G= XP_016873658.1:n.4928-357G=
XM_017018170.2:c.4715-357G= XP_016873659.1:n.4715-357G=
XM_017018171.1:c.*1235G= XP_016873660.1:n.*1235G=
XM_017018172.2:c.2600-357G= XP_016873661.1:n.2600-357G=
NM_003105.6:c.5240-357G= MANE Select NP_003096.2:n.5240-357G=