Canonical Allele Identifier: CA2039024897
Gene: AGAP2 HGNC NCBI
TSPAN31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57739420G= , CM000674.2:g.57739420G= GRCh38
NC_000012.11:g.58133203G= , CM000674.1:g.58133203G= GRCh37
NC_000012.10:g.56419470G= NCBI36
NG_029755.1:g.7742C=

Transcript Alleles

HGVS Amino-acid change
ENST00000257897.7:c.160+2492C= (AGAP2) ENSP00000257897.3:n.160+2492C=
ENST00000553221.5:n.189+1219G= (TSPAN31)
NM_014770.3:c.160+2492C= (AGAP2) NP_055585.1:n.160+2492C=
XM_005268626.1:c.160+2492C= (AGAP2) XP_005268683.1:n.160+2492C=
XM_005268626.2:c.160+2492C= (AGAP2) XP_005268683.1:n.160+2492C=
NM_014770.4:c.160+2492C= (AGAP2) NP_055585.1:n.160+2492C=
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