Canonical Allele Identifier: CA2554772674
Gene: CSTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122329858_122329884del , CM000665.2:g.122329858_122329884del GRCh38
NC_000003.11:g.122048705_122048731del , CM000665.1:g.122048705_122048731del GRCh37
NC_000003.10:g.123531395_123531421del NCBI36
NG_027995.1:g.9695_9721del

Transcript Alleles

HGVS Amino-acid change
ENST00000264474.4:c.66+4500_66+4526del MANE Select ENSP00000264474.3:n.66+4500_66+4526del
ENST00000264474.3:c.66+4500_66+4526del ENSP00000264474.3:n.66+4500_66+4526del
ENST00000479204.1:c.66+4500_66+4526del ENSP00000418891.1:n.66+4500_66+4526del
NM_005213.3:c.66+4500_66+4526del NP_005204.1:n.66+4500_66+4526del
NM_005213.4:c.66+4500_66+4526del MANE Select NP_005204.1:n.66+4500_66+4526del