Canonical Allele Identifier: CA2838225820

Gene: SRGAP3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9116433C>G , CM000665.2:g.9116433C>G	GRCh38
NC_000003.11:g.9158117C>G , CM000665.1:g.9158117C>G	GRCh37
NC_000003.10:g.9133117C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383836.8:c.260+8292G>C MANE Select	ENSP00000373347.3:n.260+8292G>C
ENST00000360413.7:c.260+8292G>C	ENSP00000353587.3:n.260+8292G>C
ENST00000383836.7:c.260+8292G>C	ENSP00000373347.3:n.260+8292G>C
ENST00000433332.7:n.329+8292G>C
ENST00000470951.5:n.300+8292G>C
ENST00000618999.4:c.-101+8292G>C	ENSP00000482666.1:n.-101+8292G>C
NM_001033117.2:c.260+8292G>C	NP_001028289.1:n.260+8292G>C
NM_014850.3:c.260+8292G>C	NP_055665.1:n.260+8292G>C
XM_011534295.1:c.260+8292G>C	XP_011532597.1:n.260+8292G>C
XM_011534296.1:c.203+8292G>C	XP_011532598.1:n.203+8292G>C
XM_011534297.1:c.-101+8292G>C	XP_011532599.1:n.-101+8292G>C
XM_011534298.1:c.-101+8292G>C	XP_011532600.1:n.-101+8292G>C
XM_011534299.1:c.-101+8292G>C	XP_011532601.1:n.-101+8292G>C
XM_011534300.1:c.-101+8292G>C	XP_011532602.1:n.-101+8292G>C
XM_011534302.1:c.260+8292G>C	XP_011532604.1:n.260+8292G>C
XR_427300.2:n.994+8292G>C
XM_011534295.2:c.260+8292G>C	XP_011532597.1:n.260+8292G>C
XM_011534296.2:c.203+8292G>C	XP_011532598.1:n.203+8292G>C
XM_017007574.1:c.314+8292G>C	XP_016863063.1:n.314+8292G>C
XM_017007575.1:c.314+8292G>C	XP_016863064.1:n.314+8292G>C
XM_017007576.2:c.-101+8292G>C	XP_016863065.1:n.-101+8292G>C
XM_017007579.1:c.314+8292G>C	XP_016863068.1:n.314+8292G>C
XM_017007580.2:c.-101+8292G>C	XP_016863069.1:n.-101+8292G>C
XM_024453842.1:c.260+8292G>C	XP_024309610.1:n.260+8292G>C
XM_024453843.1:c.-101+8292G>C	XP_024309611.1:n.-101+8292G>C
XM_024453844.1:c.-101+8292G>C	XP_024309612.1:n.-101+8292G>C
XR_001740391.1:n.1329+8292G>C
NM_014850.4:c.260+8292G>C MANE Select	NP_055665.1:n.260+8292G>C
NM_001033117.3:c.260+8292G>C	NP_001028289.1:n.260+8292G>C