Canonical Allele Identifier: CA1397899527
Gene: CSTA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325271A= , CM000665.2:g.122325271A= GRCh38
NC_000003.11:g.122044118A= , CM000665.1:g.122044118A= GRCh37
NC_000003.10:g.123526808A= NCBI36
NG_027995.1:g.5108A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.-22A= MANE Select ENSP00000264474.3:n.-22A=
ENST00000264474.3:c.-22A= ENSP00000264474.3:n.-22A=
ENST00000479204.1:c.-22A= ENSP00000418891.1:n.-22A=
NM_005213.3:c.-22A= NP_005204.1:n.-22A=
NM_005213.4:c.-22A= MANE Select NP_005204.1:n.-22A=
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