Canonical Allele Identifier: CA2619613297

Gene: SRGAP1

Linked Data

• gnomAD v4: 12-64016935-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64016939dup , CM000674.2:g.64016939dup	GRCh38
NC_000012.11:g.64410719dup , CM000674.1:g.64410719dup	GRCh37
NC_000012.10:g.62696986dup	NCBI36
NG_051659.1:g.177187dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631006.3:c.427-11dup	ENSP00000485752.2:n.427-11dup
ENST00000695902.1:c.*254-11dup	ENSP00000512252.1:n.*254-11dup
ENST00000355086.8:c.427-11dup MANE Select	ENSP00000347198.3:n.427-11dup
ENST00000355086.7:c.427-11dup	ENSP00000347198.3:n.427-11dup
ENST00000537556.1:n.441-11dup
ENST00000543397.1:c.307-11dup	ENSP00000437948.1:n.307-11dup
ENST00000631006.2:c.307-11dup	ENSP00000485752.1:n.307-11dup
NM_020762.2:c.427-11dup	NP_065813.1:n.427-11dup
XM_005269042.2:c.427-11dup	XP_005269099.1:n.427-11dup
XM_011538580.1:c.307-11dup	XP_011536882.1:n.307-11dup
XM_011538581.1:c.307-11dup	XP_011536883.1:n.307-11dup
XM_011538582.1:c.4-11dup	XP_011536884.1:n.4-11dup
XM_011538583.1:c.427-11dup	XP_011536885.1:n.427-11dup
XR_945023.1:n.896+2757dup
NM_001346201.1:c.427-11dup	NP_001333130.1:n.427-11dup
NM_020762.3:c.427-11dup	NP_065813.1:n.427-11dup
XM_011538580.2:c.307-11dup	XP_011536882.1:n.307-11dup
XM_011538581.2:c.307-11dup	XP_011536883.1:n.307-11dup
XM_024449096.1:c.427-11dup	XP_024304864.1:n.427-11dup
XM_024449097.1:c.427-11dup	XP_024304865.1:n.427-11dup
XR_945023.2:n.925+2757dup
NM_020762.4:c.427-11dup MANE Select	NP_065813.1:n.427-11dup
NM_001346201.2:c.427-11dup	NP_001333130.1:n.427-11dup