Canonical Allele Identifier: CA2619494181
Gene: AGAP2 HGNC NCBI
TSPAN31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57739622A>G , CM000674.2:g.57739622A>G GRCh38
NC_000012.11:g.58133405A>G , CM000674.1:g.58133405A>G GRCh37
NC_000012.10:g.56419672A>G NCBI36
NG_029755.1:g.7540T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000257897.7:c.160+2290T>C (AGAP2) ENSP00000257897.3:n.160+2290T>C
ENST00000553221.5:n.189+1421A>G (TSPAN31)
NM_014770.3:c.160+2290T>C (AGAP2) NP_055585.1:n.160+2290T>C
XM_005268626.1:c.160+2290T>C (AGAP2) XP_005268683.1:n.160+2290T>C
XM_005268626.2:c.160+2290T>C (AGAP2) XP_005268683.1:n.160+2290T>C
NM_014770.4:c.160+2290T>C (AGAP2) NP_055585.1:n.160+2290T>C