Canonical Allele Identifier: CA204465
Gene: CSTA HGNC NCBI

Linked Data

ClinVar Variation Id: 208472
dbSNP Id: rs747711488

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325356A>T , CM000665.2:g.122325356A>T GRCh38
NC_000003.11:g.122044203A>T , CM000665.1:g.122044203A>T GRCh37
NC_000003.10:g.123526893A>T NCBI36
NG_027995.1:g.5193A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264474.4:c.64A>T MANE Select ENSP00000264474.3:p.Lys22Ter
ENST00000264474.3:c.64A>T ENSP00000264474.3:p.Lys22Ter
ENST00000479204.1:c.64A>T ENSP00000418891.1:p.Lys22Ter
NM_005213.3:c.64A>T NP_005204.1:p.Lys22Ter
NM_005213.4:c.64A>T MANE Select NP_005204.1:p.Lys22Ter