Canonical Allele Identifier: CA1397899538
Gene: CSTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325284T= , CM000665.2:g.122325284T= GRCh38
NC_000003.11:g.122044131T= , CM000665.1:g.122044131T= GRCh37
NC_000003.10:g.123526821T= NCBI36
NG_027995.1:g.5121T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.-9T= MANE Select ENSP00000264474.3:n.-9T=
ENST00000264474.3:c.-9T= ENSP00000264474.3:n.-9T=
ENST00000479204.1:c.-9T= ENSP00000418891.1:n.-9T=
NM_005213.3:c.-9T= NP_005204.1:n.-9T=
NM_005213.4:c.-9T= MANE Select NP_005204.1:n.-9T=