Canonical Allele Identifier: CA2083161363

Gene: STARD13

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33119700C= , CM000675.2:g.33119700C=	GRCh38
NC_000013.10:g.33693837C= , CM000675.1:g.33693837C=	GRCh37
NC_000013.9:g.32591837C=	NCBI36
NG_029752.1:g.171065G=
NG_029752.2:g.562136G=

Transcript Alleles

HGVS	Amino-acid Change
NM_178006.4:c.2083-1437G= MANE Select	NP_821074.1:n.2083-1437G=
ENST00000336934.10:c.2083-1437G= MANE Select	ENSP00000338785.4:n.2083-1437G=
NM_001243466.1:c.2059-1459G=	NP_001230395.1:n.2059-1459G=
NM_001243466.2:c.2059-1459G=	NP_001230395.1:n.2059-1459G=
NM_001243474.1:c.1729-1437G=	NP_001230403.1:n.1729-1437G=
NM_001243474.2:c.1729-1437G=	NP_001230403.1:n.1729-1437G=
NM_001243476.2:c.1978-1437G=	NP_001230405.1:n.1978-1437G=
NM_001243476.3:c.1978-1437G=	NP_001230405.1:n.1978-1437G=
NM_052851.2:c.1729-1437G=	NP_443083.1:n.1729-1437G=
NM_052851.3:c.1729-1437G=	NP_443083.1:n.1729-1437G=
NM_178006.3:c.2083-1437G=	NP_821074.1:n.2083-1437G=
NM_178007.2:c.2059-1437G=	NP_821075.1:n.2059-1437G=
NM_178007.3:c.2059-1437G=	NP_821075.1:n.2059-1437G=
ENST00000255486.8:c.2059-1437G=	ENSP00000255486.4:n.2059-1437G=
ENST00000336934.9:c.2083-1437G=	ENSP00000338785.4:n.2083-1437G=
ENST00000399365.7:c.1729-1437G=	ENSP00000382300.3:n.1729-1437G=
ENST00000567873.2:c.2038-1437G=	ENSP00000456233.2:n.2038-1437G=
XM_011535298.1:c.2116-1437G=	XP_011533600.1:n.2116-1437G=
XM_011535299.1:c.1978-1437G=	XP_011533601.1:n.1978-1437G=
XM_011535299.3:c.1978-1437G=	XP_011533601.1:n.1978-1437G=
XM_017020834.2:c.2038-1437G=	XP_016876323.1:n.2038-1437G=
XM_017020835.2:c.1978-1437G=	XP_016876324.1:n.1978-1437G=
XM_024449429.1:c.1978-1437G=	XP_024305197.1:n.1978-1437G=