Canonical Allele Identifier: CA1206165671

Gene: SELP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169611253G= , CM000663.2:g.169611253G=	GRCh38
NC_000001.10:g.169580491G= , CM000663.1:g.169580491G=	GRCh37
NC_000001.9:g.167847115G=	NCBI36
NG_012125.1:g.23887C=
NG_012125.2:g.23887C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263686.11:c.1147+239C= MANE Select	ENSP00000263686.5:n.1147+239C=
ENST00000263686.10:c.1147+239C=	ENSP00000263686.5:n.1147+239C=
ENST00000367786.6:c.961+964C=	ENSP00000356760.1:n.961+964C=
ENST00000367788.6:c.961+239C=	ENSP00000356762.1:n.961+239C=
ENST00000367795.2:c.961+964C=	ENSP00000356769.2:n.961+964C=
ENST00000426706.6:c.1144+239C=	ENSP00000391694.2:n.1144+239C=
ENST00000458599.6:c.961+964C=	ENSP00000399368.2:n.961+964C=
NM_003005.3:c.1147+239C=	NP_002996.2:n.1147+239C=
XM_005245435.1:c.1147+239C=	XP_005245492.1:n.1147+239C=
XM_005245436.2:c.1147+239C=	XP_005245493.1:n.1147+239C=
XM_005245438.1:c.1147+239C=	XP_005245495.1:n.1147+239C=
XM_005245439.1:c.1147+239C=	XP_005245496.1:n.1147+239C=
XM_005245440.1:c.961+964C=	XP_005245497.1:n.961+964C=
XM_005245435.2:c.1147+239C=	XP_005245492.1:n.1147+239C=
XM_005245436.4:c.1147+239C=	XP_005245493.1:n.1147+239C=
XM_005245438.2:c.1147+239C=	XP_005245495.1:n.1147+239C=
XM_005245439.2:c.1147+239C=	XP_005245496.1:n.1147+239C=
XM_005245440.2:c.961+964C=	XP_005245497.1:n.961+964C=
NM_003005.4:c.1147+239C= MANE Select	NP_002996.2:n.1147+239C=