Canonical Allele Identifier: CA1397899530
Gene: CSTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325274_122325277delinsAAAG , CM000665.2:g.122325274_122325277delinsAAAG GRCh38
NC_000003.11:g.122044121_122044124delinsAAAG , CM000665.1:g.122044121_122044124delinsAAAG GRCh37
NC_000003.10:g.123526811_123526814delinsAAAG NCBI36
NG_027995.1:g.5111_5114delinsAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.-19_-16delinsAAAG MANE Select ENSP00000264474.3:n.-19_-16delinsAAAG
ENST00000264474.3:c.-19_-16delinsAAAG ENSP00000264474.3:n.-19_-16delinsAAAG
ENST00000479204.1:c.-19_-16delinsAAAG ENSP00000418891.1:n.-19_-16delinsAAAG
NM_005213.3:c.-19_-16delinsAAAG NP_005204.1:n.-19_-16delinsAAAG
NM_005213.4:c.-19_-16delinsAAAG MANE Select NP_005204.1:n.-19_-16delinsAAAG