Canonical Allele Identifier: CA1139773109

Gene: SELP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169594713T= , CM000663.2:g.169594713T=	GRCh38
NC_000001.10:g.169563951T= , CM000663.1:g.169563951T=	GRCh37
NC_000001.9:g.167830575T=	NCBI36
NG_012125.1:g.40427A=
NG_012125.2:g.40427A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003005.4:c.2266A= MANE Select	NP_002996.2:p.Thr756=
ENST00000263686.11:c.2266A= MANE Select	ENSP00000263686.5:p.Thr756=
NM_003005.3:c.2266A=	NP_002996.2:p.Thr756=
ENST00000263686.10:c.2266A=	ENSP00000263686.5:p.Thr756=
ENST00000367786.6:c.2080A=	ENSP00000356760.1:p.Thr694=
ENST00000367788.6:c.2080A=	ENSP00000356762.1:p.Thr694=
ENST00000426706.6:c.2263A=	ENSP00000391694.2:p.Thr755=
ENST00000458599.6:c.1714A=	ENSP00000399368.2:p.Thr572=
XM_005245435.1:c.2266A=	XP_005245492.1:p.Thr756=
XM_005245435.2:c.2266A=	XP_005245492.1:p.Thr756=
XM_005245436.2:c.2266A=	XP_005245493.1:p.Thr756=
XM_005245436.4:c.2266A=	XP_005245493.1:p.Thr756=
XM_005245438.1:c.2266A=	XP_005245495.1:p.Thr756=
XM_005245438.2:c.2266A=	XP_005245495.1:p.Thr756=
XM_005245439.1:c.2266A=	XP_005245496.1:p.Thr756=
XM_005245439.2:c.2266A=	XP_005245496.1:p.Thr756=
XM_005245440.1:c.2080A=	XP_005245497.1:p.Thr694=
XM_005245440.2:c.2080A=	XP_005245497.1:p.Thr694=