Canonical Allele Identifier: CA1201536854
Gene: SPTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158612716_158612719delinsAAAC , CM000663.2:g.158612716_158612719delinsAAAC GRCh38
NC_000001.10:g.158582506_158582509delinsAAAC , CM000663.1:g.158582506_158582509delinsAAAC GRCh37
NC_000001.9:g.156849130_156849133delinsAAAC NCBI36
NG_011474.1:g.78998_79001delinsGTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000643759.2:c.7134+98_7134+101delinsGTTT MANE Select ENSP00000495214.1:n.7134+98_7134+101delin...
ENST00000368147.8:c.7134+98_7134+101delinsGTTT ENSP00000357129.4:n.7134+98_7134+101delin...
ENST00000614909.4:c.7134+98_7134+101delinsGTTT ENSP00000482595.1:n.7134+98_7134+101delin...
NM_003126.2:c.7134+98_7134+101delinsGTTT NP_003117.2:n.7134+98_7134+101delinsGTTT
XM_011509916.1:c.7134+98_7134+101delinsGTTT XP_011508218.1:n.7134+98_7134+101delinsGT...
XM_011509917.1:c.7116+98_7116+101delinsGTTT XP_011508219.1:n.7116+98_7116+101delinsGT...
NM_003126.3:c.7134+98_7134+101delinsGTTT NP_003117.2:n.7134+98_7134+101delinsGTTT
XM_011509916.2:c.7134+98_7134+101delinsGTTT XP_011508218.1:n.7134+98_7134+101delinsGT...
XM_011509917.3:c.7116+98_7116+101delinsGTTT XP_011508219.1:n.7116+98_7116+101delinsGT...
NM_003126.4:c.7134+98_7134+101delinsGTTT MANE Select NP_003117.2:n.7134+98_7134+101delinsGTTT