Canonical Allele Identifier: CA1397901683
Gene: CSTA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122329842_122329845delinsACCT , CM000665.2:g.122329842_122329845delinsACCT GRCh38
NC_000003.11:g.122048689_122048692delinsACCT , CM000665.1:g.122048689_122048692delinsACCT GRCh37
NC_000003.10:g.123531379_123531382delinsACCT NCBI36
NG_027995.1:g.9679_9682delinsACCT

Transcript Alleles

HGVS Amino-acid change
ENST00000264474.4:c.66+4484_66+4487delinsACCT MANE Select ENSP00000264474.3:n.66+4484_66+4487delins...
ENST00000264474.3:c.66+4484_66+4487delinsACCT ENSP00000264474.3:n.66+4484_66+4487delins...
ENST00000479204.1:c.66+4484_66+4487delinsACCT ENSP00000418891.1:n.66+4484_66+4487delins...
NM_005213.3:c.66+4484_66+4487delinsACCT NP_005204.1:n.66+4484_66+4487delinsACCT
NM_005213.4:c.66+4484_66+4487delinsACCT MANE Select NP_005204.1:n.66+4484_66+4487delinsACCT
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