Canonical Allele Identifier: CA2039024957
Gene: AGAP2 HGNC NCBI
TSPAN31 HGNC NCBI

Linked Data

dbSNP Id: rs1955050590

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57739481_57739483del , CM000674.2:g.57739481_57739483del GRCh38
NC_000012.11:g.58133264_58133266del , CM000674.1:g.58133264_58133266del GRCh37
NC_000012.10:g.56419531_56419533del NCBI36
NG_029755.1:g.7681_7683del

Transcript Alleles

HGVS Amino-acid Change
ENST00000257897.7:c.160+2431_160+2433del (AGAP2) ENSP00000257897.3:n.160+2431_160+2433del
ENST00000553221.5:n.189+1280_189+1282del (TSPAN31)
NM_014770.3:c.160+2431_160+2433del (AGAP2) NP_055585.1:n.160+2431_160+2433del
XM_005268626.1:c.160+2431_160+2433del (AGAP2) XP_005268683.1:n.160+2431_160+2433del
XM_005268626.2:c.160+2431_160+2433del (AGAP2) XP_005268683.1:n.160+2431_160+2433del
NM_014770.4:c.160+2431_160+2433del (AGAP2) NP_055585.1:n.160+2431_160+2433del