Canonical Allele Identifier: CA1206166800

Gene: SELP

Linked Data

• dbSNP Id: rs3917751

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169607330G>T , CM000663.2:g.169607330G>T	GRCh38
NC_000001.10:g.169576568G>T , CM000663.1:g.169576568G>T	GRCh37
NC_000001.9:g.167843192G>T	NCBI36
NG_012125.1:g.27810C>A
NG_012125.2:g.27810C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263686.11:c.1334-196C>A MANE Select	ENSP00000263686.5:n.1334-196C>A
ENST00000263686.10:c.1334-196C>A	ENSP00000263686.5:n.1334-196C>A
ENST00000367786.6:c.1148-196C>A	ENSP00000356760.1:n.1148-196C>A
ENST00000367788.6:c.1148-196C>A	ENSP00000356762.1:n.1148-196C>A
ENST00000367795.2:c.962-196C>A	ENSP00000356769.2:n.962-196C>A
ENST00000426706.6:c.1331-196C>A	ENSP00000391694.2:n.1331-196C>A
ENST00000458599.6:c.1148-196C>A	ENSP00000399368.2:n.1148-196C>A
NM_003005.3:c.1334-196C>A	NP_002996.2:n.1334-196C>A
XM_005245435.1:c.1334-196C>A	XP_005245492.1:n.1334-196C>A
XM_005245436.2:c.1334-196C>A	XP_005245493.1:n.1334-196C>A
XM_005245438.1:c.1334-196C>A	XP_005245495.1:n.1334-196C>A
XM_005245439.1:c.1334-196C>A	XP_005245496.1:n.1334-196C>A
XM_005245440.1:c.1148-196C>A	XP_005245497.1:n.1148-196C>A
XM_005245435.2:c.1334-196C>A	XP_005245492.1:n.1334-196C>A
XM_005245436.4:c.1334-196C>A	XP_005245493.1:n.1334-196C>A
XM_005245438.2:c.1334-196C>A	XP_005245495.1:n.1334-196C>A
XM_005245439.2:c.1334-196C>A	XP_005245496.1:n.1334-196C>A
XM_005245440.2:c.1148-196C>A	XP_005245497.1:n.1148-196C>A
NM_003005.4:c.1334-196C>A MANE Select	NP_002996.2:n.1334-196C>A