Canonical Allele Identifier: CA383038922
Gene: SORL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121605233A>C , CM000673.2:g.121605233A>C GRCh38
NC_000011.9:g.121475942A>C , CM000673.1:g.121475942A>C GRCh37
NC_000011.8:g.120981152A>C NCBI36
NG_023313.1:g.157982A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260197.12:c.4772A>C MANE Select ENSP00000260197.6:p.Tyr1591Ser
ENST00000260197.11:c.4772A>C ENSP00000260197.6:p.Tyr1591Ser
ENST00000525532.5:c.1604A>C ENSP00000434634.1:p.Tyr535Ser
ENST00000527934.1:c.617A>C ENSP00000435405.1:p.Tyr206Ser
ENST00000532694.5:c.1310A>C ENSP00000432131.1:p.Tyr437Ser
ENST00000534286.5:c.1502A>C ENSP00000436447.1:p.Tyr501Ser
NM_003105.5:c.4772A>C NP_003096.1:p.Tyr1591Ser
XM_011542963.1:c.4658A>C XP_011541265.1:p.Tyr1553Ser
XM_011542964.1:c.4772A>C XP_011541266.1:p.Tyr1591Ser
XM_011542965.1:c.3233A>C XP_011541267.1:p.Tyr1078Ser
XM_011542966.1:c.2132A>C XP_011541268.1:p.Tyr711Ser
XM_011542967.1:c.1604A>C XP_011541269.1:p.Tyr535Ser
XM_011542963.3:c.4658A>C XP_011541265.1:p.Tyr1553Ser
XM_011542965.3:c.3233A>C XP_011541267.1:p.Tyr1078Ser
XM_011542967.3:c.1604A>C XP_011541269.1:p.Tyr535Ser
XM_017018169.2:c.4460A>C XP_016873658.1:p.Tyr1487Ser
XM_017018170.2:c.4247A>C XP_016873659.1:p.Tyr1416Ser
XM_017018171.1:c.4772A>C XP_016873660.1:p.Tyr1591Ser
XM_017018172.2:c.2132A>C XP_016873661.1:p.Tyr711Ser
NM_003105.6:c.4772A>C MANE Select NP_003096.2:p.Tyr1591Ser