Canonical Allele Identifier: CA1436388116
Gene: SORCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.7478537_7478538delinsGT , CM000666.2:g.7478537_7478538delinsGT GRCh38
NC_000004.11:g.7480264_7480265delinsGT , CM000666.1:g.7480264_7480265delinsGT GRCh37
NC_000004.10:g.7531164_7531165delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329016.10:c.33-52993_33-52992delinsGT ENSP00000329124.10:n.33-52993_33-52992delinsGT
ENST00000507866.6:c.549-52993_549-52992delinsGT MANE Select ENSP00000422185.2:n.549-52993_549-52992delinsGT
ENST00000511199.1:n.164-52993_164-52992delinsGT
NM_020777.2:c.549-52993_549-52992delinsGT NP_065828.2:n.549-52993_549-52992delinsGT
XM_005247987.3:c.549-52993_549-52992delinsGT XP_005248044.2:n.549-52993_549-52992delinsGT
XM_011513514.1:c.549-52993_549-52992delinsGT XP_011511816.1:n.549-52993_549-52992delinsGT
XM_011513515.1:c.549-52993_549-52992delinsGT XP_011511817.1:n.549-52993_549-52992delinsGT
XM_011513516.1:c.549-52993_549-52992delinsGT XP_011511818.1:n.549-52993_549-52992delinsGT
XM_011513517.1:c.156-52993_156-52992delinsGT XP_011511819.1:n.156-52993_156-52992delinsGT
XM_005247987.4:c.549-52993_549-52992delinsGT XP_005248044.2:n.549-52993_549-52992delinsGT
XM_011513514.2:c.549-52993_549-52992delinsGT XP_011511816.1:n.549-52993_549-52992delinsGT
XM_011513515.2:c.549-52993_549-52992delinsGT XP_011511817.1:n.549-52993_549-52992delinsGT
XM_011513516.2:c.549-52993_549-52992delinsGT XP_011511818.1:n.549-52993_549-52992delinsGT
XM_017008481.1:c.549-52993_549-52992delinsGT XP_016863970.1:n.549-52993_549-52992delinsGT
NM_020777.3:c.549-52993_549-52992delinsGT MANE Select NP_065828.2:n.549-52993_549-52992delinsGT