Canonical Allele Identifier: CA2200991105

Gene: AXIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.342392C= , CM000678.2:g.342392C=	GRCh38
NC_000016.9:g.392392C= , CM000678.1:g.392392C=	GRCh37
NC_000016.8:g.332393C=	NCBI36
NG_012267.1:g.15073G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262320.8:c.878+3756G= MANE Select	ENSP00000262320.3:n.878+3756G=
ENST00000262320.7:c.878+3756G=	ENSP00000262320.3:n.878+3756G=
ENST00000354866.7:c.878+3756G=	ENSP00000346935.3:n.878+3756G=
ENST00000461023.5:n.175+3756G=
ENST00000481769.1:n.305+9977G=
NM_003502.3:c.878+3756G=	NP_003493.1:n.878+3756G=
NM_181050.2:c.878+3756G=	NP_851393.1:n.878+3756G=
XM_011522682.1:c.1025+3756G=	XP_011520984.1:n.1025+3756G=
XM_011522683.1:c.1025+3756G=	XP_011520985.1:n.1025+3756G=
XM_011522684.1:c.878+3756G=	XP_011520986.1:n.878+3756G=
XM_011522685.1:c.62+12666G=	XP_011520987.1:n.62+12666G=
XM_011522687.1:c.62+12666G=	XP_011520989.1:n.62+12666G=
XM_011522688.1:c.-1120+3756G=	XP_011520990.1:n.-1120+3756G=
NR_134879.1:n.1267+3756G=
XM_011522682.2:c.1025+3756G=	XP_011520984.1:n.1025+3756G=
XM_011522683.2:c.1025+3756G=	XP_011520985.1:n.1025+3756G=
XM_011522684.2:c.878+3756G=	XP_011520986.1:n.878+3756G=
XM_017023743.1:c.1025+3756G=	XP_016879232.1:n.1025+3756G=
XM_017023744.1:c.1025+3756G=	XP_016879233.1:n.1025+3756G=
XM_017023747.1:c.1025+3756G=	XP_016879236.1:n.1025+3756G=
XM_017023748.1:c.1025+3756G=	XP_016879237.1:n.1025+3756G=
XR_001751996.1:n.1280+3756G=
NM_003502.4:c.878+3756G= MANE Select	NP_003493.1:n.878+3756G=
NM_181050.3:c.878+3756G=	NP_851393.1:n.878+3756G=
NR_134879.2:n.1314+3756G=