Canonical Allele Identifier: CA373788980

Gene: SPTLC1

Linked Data

• MyVariant Identifiers: chr9:g.94794781G>C (hg19) ; chr9:g.92032499G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92032499G>C , CM000671.2:g.92032499G>C	GRCh38
NC_000009.11:g.94794781G>C , CM000671.1:g.94794781G>C	GRCh37
NC_000009.10:g.93834602G>C	NCBI36
NG_007950.1:g.87910C>G , LRG_272:g.87910C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686600.1:c.*100C>G	ENSP00000509268.1:n.*100C>G
ENST00000686799.1:n.1712C>G
ENST00000687427.1:c.*144C>G	ENSP00000509426.1:n.*144C>G
ENST00000687817.1:c.*3786C>G	ENSP00000508926.1:n.*3786C>G
ENST00000687972.1:c.1448C>G	ENSP00000509208.1:p.Thr483Ser
ENST00000689261.1:n.1295C>G
ENST00000689401.1:c.*1638C>G	ENSP00000510251.1:n.*1638C>G
ENST00000690095.1:n.1776C>G
ENST00000690139.1:c.*1089C>G	ENSP00000510483.1:n.*1089C>G
ENST00000692458.1:n.2026C>G
ENST00000262554.7:c.1388C>G MANE Select	ENSP00000262554.2:p.Thr463Ser
ENST00000642671.1:c.1629+2311C>G	ENSP00000495764.1:n.1629+2311C>G
ENST00000643599.1:c.1396+2311C>G	ENSP00000494770.1:n.1396+2311C>G
ENST00000644140.1:c.*1129C>G	ENSP00000493933.1:n.*1129C>G
ENST00000646481.1:c.1260+2311C>G	ENSP00000496627.1:n.1260+2311C>G
ENST00000646534.1:c.*1191C>G	ENSP00000495388.1:n.*1191C>G
ENST00000262554.6:c.1388C>G	ENSP00000262554.2:p.Thr463Ser
ENST00000469778.1:n.345C>G
NM_001281303.1:c.1356C>G	NP_001268232.1:p.His452Gln
NM_006415.3:c.1388C>G	NP_006406.1:p.Thr463Ser
XM_011518139.1:c.923C>G	XP_011516441.1:p.Thr308Ser
XM_011518139.3:c.923C>G	XP_011516441.1:p.Thr308Ser
XM_017014200.2:c.1022C>G	XP_016869689.1:p.Thr341Ser
XM_017014201.2:c.1022C>G	XP_016869690.1:p.Thr341Ser
XM_024447378.1:c.923C>G	XP_024303146.1:p.Thr308Ser
XM_024447379.1:c.923C>G	XP_024303147.1:p.Thr308Ser
XR_002956744.1:n.1538C>G
NM_006415.4:c.1388C>G MANE Select	NP_006406.1:p.Thr463Ser
NM_001281303.2:c.1356C>G	NP_001268232.1:p.His452Gln
NM_001368272.1:c.1022C>G	NP_001355201.1:p.Thr341Ser
NM_001368273.1:c.923C>G	NP_001355202.1:p.Thr308Ser