Canonical Allele Identifier: CA2083221060

Gene: STARD13

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33224066G= , CM000675.2:g.33224066G=	GRCh38
NC_000013.10:g.33798203G= , CM000675.1:g.33798203G=	GRCh37
NC_000013.9:g.32696203G=	NCBI36
NG_029752.1:g.66699C=
NG_029752.2:g.457770C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567873.2:c.125-56444C=	ENSP00000456233.2:n.125-56444C=
ENST00000336934.10:c.170-56444C= MANE Select	ENSP00000338785.4:n.170-56444C=
ENST00000336934.9:c.170-56444C=	ENSP00000338785.4:n.170-56444C=
ENST00000487412.5:n.287-56444C=
ENST00000498019.2:n.239-56444C=
ENST00000567873.1:c.125-56444C=	ENSP00000456233.1:n.125-56444C=
NM_001243476.2:c.65-56444C=	NP_001230405.1:n.65-56444C=
NM_178006.3:c.170-56444C=	NP_821074.1:n.170-56444C=
XM_011535298.1:c.203-56444C=	XP_011533600.1:n.203-56444C=
XM_011535299.1:c.65-56444C=	XP_011533601.1:n.65-56444C=
XM_011535299.3:c.65-56444C=	XP_011533601.1:n.65-56444C=
XM_017020834.2:c.125-56444C=	XP_016876323.1:n.125-56444C=
XM_017020835.2:c.65-56444C=	XP_016876324.1:n.65-56444C=
XM_024449429.1:c.65-56444C=	XP_024305197.1:n.65-56444C=
NM_178006.4:c.170-56444C= MANE Select	NP_821074.1:n.170-56444C=
NM_001243476.3:c.65-56444C=	NP_001230405.1:n.65-56444C=