Canonical Allele Identifier: CA2039025038
Gene: AGAP2 HGNC NCBI
TSPAN31 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57739546C= , CM000674.2:g.57739546C= GRCh38
NC_000012.11:g.58133329C= , CM000674.1:g.58133329C= GRCh37
NC_000012.10:g.56419596C= NCBI36
NG_029755.1:g.7616G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257897.7:c.160+2366G= (AGAP2) ENSP00000257897.3:n.160+2366G=
ENST00000553221.5:n.189+1345C= (TSPAN31)
NM_014770.3:c.160+2366G= (AGAP2) NP_055585.1:n.160+2366G=
XM_005268626.1:c.160+2366G= (AGAP2) XP_005268683.1:n.160+2366G=
XM_005268626.2:c.160+2366G= (AGAP2) XP_005268683.1:n.160+2366G=
NM_014770.4:c.160+2366G= (AGAP2) NP_055585.1:n.160+2366G=
Search 100 bp 5'
Search 100 bp 3'