Canonical Allele Identifier: CA1139797098

Gene: SORT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109313684G= , CM000663.2:g.109313684G=	GRCh38
NC_000001.10:g.109856306G= , CM000663.1:g.109856306G=	GRCh37
NC_000001.9:g.109657829G=	NCBI36
NG_028280.1:g.89258C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256637.8:c.*359C= MANE Select	ENSP00000256637.6:n.*359C=
ENST00000256637.7:c.*359C=	ENSP00000256637.6:n.*359C=
ENST00000538502.5:c.*359C=	ENSP00000438597.1:n.*359C=
NM_001205228.1:c.*359C=	NP_001192157.1:n.*359C=
NM_002959.5:c.*359C=	NP_002950.3:n.*359C=
NM_002959.6:c.*359C=	NP_002950.3:n.*359C=
XM_005271100.2:c.*359C=	XP_005271157.1:n.*359C=
XM_005271101.1:c.*359C=	XP_005271158.1:n.*359C=
XM_005271102.1:c.*359C=	XP_005271159.1:n.*359C=
XM_006710812.1:c.*359C=	XP_006710875.1:n.*359C=
XM_005271101.3:c.*359C=	XP_005271158.1:n.*359C=
XM_005271102.2:c.*359C=	XP_005271159.1:n.*359C=
XM_006710812.2:c.*359C=	XP_006710875.1:n.*359C=
NM_002959.7:c.*359C= MANE Select	NP_002950.3:n.*359C=
NM_001205228.2:c.*359C=	NP_001192157.1:n.*359C=