Canonical Allele Identifier: CA515423584

Gene: SMS

Linked Data

• MyVariant Identifiers: chrX:g.21997042G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.21978924G>C , CM000685.2:g.21978924G>C	GRCh38
NC_000023.10:g.21997042G>C , CM000685.1:g.21997042G>C	GRCh37
NC_000023.9:g.21906963G>C	NCBI36
NG_009228.1:g.43201G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404933.7:c.708G>C MANE Select	ENSP00000385746.2:p.Thr236=
ENST00000379404.5:c.549G>C	ENSP00000368714.1:p.Thr183=
ENST00000404933.6:c.708G>C	ENSP00000385746.2:p.Thr236=
NM_001258423.1:c.549G>C	NP_001245352.1:p.Thr183=
NM_004595.4:c.708G>C	NP_004586.2:p.Thr236=
XM_005274582.1:c.606G>C	XP_005274639.1:p.Thr202=
XM_011545568.1:c.606G>C	XP_011543870.1:p.Thr202=
XM_005274582.2:c.606G>C	XP_005274639.1:p.Thr202=
XM_011545568.2:c.606G>C	XP_011543870.1:p.Thr202=
XM_017029753.2:c.708G>C	XP_016885242.1:p.Thr236=
XM_017029754.1:c.606G>C	XP_016885243.1:p.Thr202=
XM_017029755.1:c.606G>C	XP_016885244.1:p.Thr202=
XM_024452427.1:c.606G>C	XP_024308195.1:p.Thr202=
NM_004595.5:c.708G>C MANE Select	NP_004586.2:p.Thr236=
NM_001258423.2:c.549G>C	NP_001245352.1:p.Thr183=