Canonical Allele Identifier: CA1148890165
Gene: SPTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158612731_158612736delinsTTTTTT , CM000663.2:g.158612731_158612736delinsTTTTTT GRCh38
NC_000001.10:g.158582521_158582526delinsTTTTTT , CM000663.1:g.158582521_158582526delinsTTTTTT GRCh37
NC_000001.9:g.156849145_156849150delinsTTTTTT NCBI36
NG_011474.1:g.78981_78986delinsAAAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000643759.2:c.7134+81_7134+86delinsAAAAAA MANE Select ENSP00000495214.1:n.7134+81_7134+86delins...
ENST00000368147.8:c.7134+81_7134+86delinsAAAAAA ENSP00000357129.4:n.7134+81_7134+86delins...
ENST00000614909.4:c.7134+81_7134+86delinsAAAAAA ENSP00000482595.1:n.7134+81_7134+86delins...
NM_003126.2:c.7134+81_7134+86delinsAAAAAA NP_003117.2:n.7134+81_7134+86delinsAAAAAA...
XM_011509916.1:c.7134+81_7134+86delinsAAAAAA XP_011508218.1:n.7134+81_7134+86delinsAAA...
XM_011509917.1:c.7116+81_7116+86delinsAAAAAA XP_011508219.1:n.7116+81_7116+86delinsAAA...
NM_003126.3:c.7134+81_7134+86delinsAAAAAA NP_003117.2:n.7134+81_7134+86delinsAAAAAA...
XM_011509916.2:c.7134+81_7134+86delinsAAAAAA XP_011508218.1:n.7134+81_7134+86delinsAAA...
XM_011509917.3:c.7116+81_7116+86delinsAAAAAA XP_011508219.1:n.7116+81_7116+86delinsAAA...
NM_003126.4:c.7134+81_7134+86delinsAAAAAA MANE Select NP_003117.2:n.7134+81_7134+86delinsAAAAAA...