Canonical Allele Identifier: CA1957686529

Gene: GAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22808272A= , CM000673.2:g.22808272A=	GRCh38
NC_000011.9:g.22829818A= , CM000673.1:g.22829818A=	GRCh37
NC_000011.8:g.22786394A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454584.7:c.724-3526A= MANE Select	ENSP00000401145.2:n.724-3526A=
ENST00000278187.7:c.724-3526A=	ENSP00000278187.3:n.724-3526A=
ENST00000454584.6:c.724-3526A=	ENSP00000401145.2:n.724-3526A=
ENST00000524701.5:c.*364-3526A=	ENSP00000432026.1:n.*364-3526A=
NM_001143830.1:c.724-3526A=	NP_001137302.1:n.724-3526A=
NM_005256.3:c.724-3526A=	NP_005247.1:n.724-3526A=
NM_177553.2:c.724-3526A=	NP_808221.1:n.724-3526A=
XM_011519971.1:c.778-3526A=	XP_011518273.1:n.778-3526A=
XM_011519972.1:c.778-3526A=	XP_011518274.1:n.778-3526A=
XM_011519973.1:c.778-3526A=	XP_011518275.1:n.778-3526A=
XM_011519978.1:c.*20-3526A=	XP_011518280.1:n.*20-3526A=
NM_001351224.1:c.*20-3526A=	NP_001338153.1:n.*20-3526A=
NR_147085.1:n.1168-3526A=
XM_011519971.3:c.778-3526A=	XP_011518273.1:n.778-3526A=
XM_011519972.3:c.778-3526A=	XP_011518274.1:n.778-3526A=
XM_017017532.1:c.724-26635A=	XP_016873021.1:n.724-26635A=
XR_001747829.1:n.1030-26635A=
NM_001143830.2:c.724-3526A=	NP_001137302.1:n.724-3526A=
NM_001351224.2:c.*20-3526A=	NP_001338153.1:n.*20-3526A=
NM_005256.4:c.724-3526A=	NP_005247.1:n.724-3526A=
NM_177553.3:c.724-3526A=	NP_808221.1:n.724-3526A=
NR_147085.2:n.1436-3526A=
NM_001143830.3:c.724-3526A= MANE Select	NP_001137302.1:n.724-3526A=
NM_001351224.3:c.*20-3526A=	NP_001338153.1:n.*20-3526A=
NM_001391933.1:c.778-3526A=	NP_001378862.1:n.778-3526A=
NM_001391934.1:c.724-3526A=	NP_001378863.1:n.724-3526A=
NM_001391935.1:c.724-3526A=	NP_001378864.1:n.724-3526A=
NM_001391936.1:c.724-3526A=	NP_001378865.1:n.724-3526A=
NM_001391937.1:c.724-3526A=	NP_001378866.1:n.724-3526A=
NM_005256.5:c.724-3526A=	NP_005247.1:n.724-3526A=
NM_177553.4:c.724-3526A=	NP_808221.1:n.724-3526A=