Canonical Allele Identifier: CA1397899534
Gene: CSTA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325279A= , CM000665.2:g.122325279A= GRCh38
NC_000003.11:g.122044126A= , CM000665.1:g.122044126A= GRCh37
NC_000003.10:g.123526816A= NCBI36
NG_027995.1:g.5116A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264474.4:c.-14A= MANE Select ENSP00000264474.3:n.-14A=
ENST00000264474.3:c.-14A= ENSP00000264474.3:n.-14A=
ENST00000479204.1:c.-14A= ENSP00000418891.1:n.-14A=
NM_005213.3:c.-14A= NP_005204.1:n.-14A=
NM_005213.4:c.-14A= MANE Select NP_005204.1:n.-14A=
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