Canonical Allele Identifier: CA2039025025
Gene: AGAP2 HGNC NCBI
TSPAN31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57739539T= , CM000674.2:g.57739539T= GRCh38
NC_000012.11:g.58133322T= , CM000674.1:g.58133322T= GRCh37
NC_000012.10:g.56419589T= NCBI36
NG_029755.1:g.7623A=

Transcript Alleles

HGVS Amino-acid change
ENST00000257897.7:c.160+2373A= (AGAP2) ENSP00000257897.3:n.160+2373A=
ENST00000553221.5:n.189+1338T= (TSPAN31)
NM_014770.3:c.160+2373A= (AGAP2) NP_055585.1:n.160+2373A=
XM_005268626.1:c.160+2373A= (AGAP2) XP_005268683.1:n.160+2373A=
XM_005268626.2:c.160+2373A= (AGAP2) XP_005268683.1:n.160+2373A=
NM_014770.4:c.160+2373A= (AGAP2) NP_055585.1:n.160+2373A=
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