Canonical Allele Identifier: CA2041977402

Gene: SRGAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64016889T= , CM000674.2:g.64016889T=	GRCh38
NC_000012.11:g.64410669T= , CM000674.1:g.64410669T=	GRCh37
NC_000012.10:g.62696936T=	NCBI36
NG_051659.1:g.177137T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000631006.3:c.427-61T=	ENSP00000485752.2:n.427-61T=
ENST00000695902.1:c.*254-61T=	ENSP00000512252.1:n.*254-61T=
ENST00000355086.8:c.427-61T= MANE Select	ENSP00000347198.3:n.427-61T=
ENST00000355086.7:c.427-61T=	ENSP00000347198.3:n.427-61T=
ENST00000537556.1:n.441-61T=
ENST00000543397.1:c.307-61T=	ENSP00000437948.1:n.307-61T=
ENST00000631006.2:c.307-61T=	ENSP00000485752.1:n.307-61T=
NM_020762.2:c.427-61T=	NP_065813.1:n.427-61T=
XM_005269042.2:c.427-61T=	XP_005269099.1:n.427-61T=
XM_011538580.1:c.307-61T=	XP_011536882.1:n.307-61T=
XM_011538581.1:c.307-61T=	XP_011536883.1:n.307-61T=
XM_011538582.1:c.4-61T=	XP_011536884.1:n.4-61T=
XM_011538583.1:c.427-61T=	XP_011536885.1:n.427-61T=
XR_945023.1:n.896+2804A=
NM_001346201.1:c.427-61T=	NP_001333130.1:n.427-61T=
NM_020762.3:c.427-61T=	NP_065813.1:n.427-61T=
XM_011538580.2:c.307-61T=	XP_011536882.1:n.307-61T=
XM_011538581.2:c.307-61T=	XP_011536883.1:n.307-61T=
XM_024449096.1:c.427-61T=	XP_024304864.1:n.427-61T=
XM_024449097.1:c.427-61T=	XP_024304865.1:n.427-61T=
XR_945023.2:n.925+2804A=
NM_020762.4:c.427-61T= MANE Select	NP_065813.1:n.427-61T=
NM_001346201.2:c.427-61T=	NP_001333130.1:n.427-61T=