Canonical Allele Identifier: CA2577870150
Gene: CSTA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122325285C>T , CM000665.2:g.122325285C>T GRCh38
NC_000003.11:g.122044132C>T , CM000665.1:g.122044132C>T GRCh37
NC_000003.10:g.123526822C>T NCBI36
NG_027995.1:g.5122C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264474.4:c.-8C>T MANE Select ENSP00000264474.3:n.-8C>T
ENST00000264474.3:c.-8C>T ENSP00000264474.3:n.-8C>T
ENST00000479204.1:c.-8C>T ENSP00000418891.1:n.-8C>T
NM_005213.3:c.-8C>T NP_005204.1:n.-8C>T
NM_005213.4:c.-8C>T MANE Select NP_005204.1:n.-8C>T