Canonical Allele Identifier: CA690314570
Gene: AGAP2 HGNC NCBI
TSPAN31 HGNC NCBI

Linked Data

dbSNP Id: rs560045668

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57739545G>A , CM000674.2:g.57739545G>A GRCh38
NC_000012.11:g.58133328G>A , CM000674.1:g.58133328G>A GRCh37
NC_000012.10:g.56419595G>A NCBI36
NG_029755.1:g.7617C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000257897.7:c.160+2367C>T (AGAP2) ENSP00000257897.3:n.160+2367C>T
ENST00000553221.5:n.189+1344G>A (TSPAN31)
NM_014770.3:c.160+2367C>T (AGAP2) NP_055585.1:n.160+2367C>T
XM_005268626.1:c.160+2367C>T (AGAP2) XP_005268683.1:n.160+2367C>T
XM_005268626.2:c.160+2367C>T (AGAP2) XP_005268683.1:n.160+2367C>T
NM_014770.4:c.160+2367C>T (AGAP2) NP_055585.1:n.160+2367C>T