Canonical Allele Identifier: CA515453962

Gene: SAT1

Linked Data

• MyVariant Identifiers: chrX:g.23801498T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.23783381T>C , CM000685.2:g.23783381T>C	GRCh38
NC_000023.10:g.23801498T>C , CM000685.1:g.23801498T>C	GRCh37
NC_000023.9:g.23711419T>C	NCBI36
NG_012929.1:g.5224T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379270.5:c.30T>C MANE Select	ENSP00000368572.4:p.Thr10=
ENST00000379251.7:c.30T>C	ENSP00000368553.3:p.Thr10=
ENST00000379253.7:c.30T>C	ENSP00000368555.3:p.Thr10=
ENST00000379254.5:c.30T>C	ENSP00000368556.1:p.Thr10=
ENST00000379270.4:c.30T>C	ENSP00000368572.4:p.Thr10=
ENST00000463236.5:n.45T>C
ENST00000489394.5:n.185T>C
NM_002970.3:c.30T>C	NP_002961.1:p.Thr10=
NR_027783.2:n.224T>C
XM_024452421.1:c.-1310T>C	XP_024308189.1:n.-1310T>C
NM_002970.4:c.30T>C MANE Select	NP_002961.1:p.Thr10=
NR_027783.3:n.209T>C