Canonical Allele Identifier: CA343149877

Gene: SELP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169594712G>C , CM000663.2:g.169594712G>C	GRCh38
NC_000001.10:g.169563950G>C , CM000663.1:g.169563950G>C	GRCh37
NC_000001.9:g.167830574G>C	NCBI36
NG_012125.1:g.40428C>G
NG_012125.2:g.40428C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003005.4:c.2267C>G MANE Select	NP_002996.2:p.Thr756Ser
ENST00000263686.11:c.2267C>G MANE Select	ENSP00000263686.5:p.Thr756Ser
NM_003005.3:c.2267C>G	NP_002996.2:p.Thr756Ser
ENST00000263686.10:c.2267C>G	ENSP00000263686.5:p.Thr756Ser
ENST00000367786.6:c.2081C>G	ENSP00000356760.1:p.Thr694Ser
ENST00000367788.6:c.2081C>G	ENSP00000356762.1:p.Thr694Ser
ENST00000426706.6:c.2264C>G	ENSP00000391694.2:p.Thr755Ser
ENST00000458599.6:c.1715C>G	ENSP00000399368.2:p.Thr572Ser
XM_005245435.1:c.2267C>G	XP_005245492.1:p.Thr756Ser
XM_005245435.2:c.2267C>G	XP_005245492.1:p.Thr756Ser
XM_005245436.2:c.2267C>G	XP_005245493.1:p.Thr756Ser
XM_005245436.4:c.2267C>G	XP_005245493.1:p.Thr756Ser
XM_005245438.1:c.2267C>G	XP_005245495.1:p.Thr756Ser
XM_005245438.2:c.2267C>G	XP_005245495.1:p.Thr756Ser
XM_005245439.1:c.2267C>G	XP_005245496.1:p.Thr756Ser
XM_005245439.2:c.2267C>G	XP_005245496.1:p.Thr756Ser
XM_005245440.1:c.2081C>G	XP_005245497.1:p.Thr694Ser
XM_005245440.2:c.2081C>G	XP_005245497.1:p.Thr694Ser