Canonical Allele Identifier: CA412531288

Gene: SAT1

Linked Data

• MyVariant Identifiers: chrX:g.23801500C>A (hg19) ; chrX:g.23783383C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.23783383C>A , CM000685.2:g.23783383C>A	GRCh38
NC_000023.10:g.23801500C>A , CM000685.1:g.23801500C>A	GRCh37
NC_000023.9:g.23711421C>A	NCBI36
NG_012929.1:g.5226C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000379270.5:c.32C>A MANE Select	ENSP00000368572.4:p.Ala11Asp
ENST00000379251.7:c.32C>A	ENSP00000368553.3:p.Ala11Asp
ENST00000379253.7:c.32C>A	ENSP00000368555.3:p.Ala11Asp
ENST00000379254.5:c.32C>A	ENSP00000368556.1:p.Ala11Asp
ENST00000379270.4:c.32C>A	ENSP00000368572.4:p.Ala11Asp
ENST00000463236.5:n.47C>A
ENST00000489394.5:n.187C>A
NM_002970.3:c.32C>A	NP_002961.1:p.Ala11Asp
NR_027783.2:n.226C>A
XM_024452421.1:c.-1308C>A	XP_024308189.1:n.-1308C>A
NM_002970.4:c.32C>A MANE Select	NP_002961.1:p.Ala11Asp
NR_027783.3:n.211C>A