Canonical Allele Identifier: CA383038889

Gene: SORL1

Linked Data

• MyVariant Identifiers: chr11:g.121475930T>C (hg19) ; chr11:g.121605221T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121605221T>C , CM000673.2:g.121605221T>C	GRCh38
NC_000011.9:g.121475930T>C , CM000673.1:g.121475930T>C	GRCh37
NC_000011.8:g.120981140T>C	NCBI36
NG_023313.1:g.157970T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260197.12:c.4760T>C MANE Select	ENSP00000260197.6:p.Val1587Ala
ENST00000260197.11:c.4760T>C	ENSP00000260197.6:p.Val1587Ala
ENST00000525532.5:c.1592T>C	ENSP00000434634.1:p.Val531Ala
ENST00000527934.1:c.605T>C	ENSP00000435405.1:p.Val202Ala
ENST00000532694.5:c.1298T>C	ENSP00000432131.1:p.Val433Ala
ENST00000534286.5:c.1490T>C	ENSP00000436447.1:p.Val497Ala
NM_003105.5:c.4760T>C	NP_003096.1:p.Val1587Ala
XM_011542963.1:c.4646T>C	XP_011541265.1:p.Val1549Ala
XM_011542964.1:c.4760T>C	XP_011541266.1:p.Val1587Ala
XM_011542965.1:c.3221T>C	XP_011541267.1:p.Val1074Ala
XM_011542966.1:c.2120T>C	XP_011541268.1:p.Val707Ala
XM_011542967.1:c.1592T>C	XP_011541269.1:p.Val531Ala
XM_011542963.3:c.4646T>C	XP_011541265.1:p.Val1549Ala
XM_011542965.3:c.3221T>C	XP_011541267.1:p.Val1074Ala
XM_011542967.3:c.1592T>C	XP_011541269.1:p.Val531Ala
XM_017018169.2:c.4448T>C	XP_016873658.1:p.Val1483Ala
XM_017018170.2:c.4235T>C	XP_016873659.1:p.Val1412Ala
XM_017018171.1:c.4760T>C	XP_016873660.1:p.Val1587Ala
XM_017018172.2:c.2120T>C	XP_016873661.1:p.Val707Ala
NM_003105.6:c.4760T>C MANE Select	NP_003096.2:p.Val1587Ala