Canonical Allele Identifier: CA2200981670

Gene: AXIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.325782C= , CM000678.2:g.325782C=	GRCh38
NC_000016.9:g.375782C= , CM000678.1:g.375782C=	GRCh37
NC_000016.8:g.315783C=	NCBI36
NG_012267.1:g.31683G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003502.4:c.879-11099G= MANE Select	NP_003493.1:n.879-11099G=
ENST00000262320.8:c.879-11099G= MANE Select	ENSP00000262320.3:n.879-11099G=
NM_003502.3:c.879-11099G=	NP_003493.1:n.879-11099G=
NM_181050.2:c.879-11099G=	NP_851393.1:n.879-11099G=
NM_181050.3:c.879-11099G=	NP_851393.1:n.879-11099G=
NR_134879.1:n.1268-11099G=
NR_134879.2:n.1315-11099G=
ENST00000262320.7:c.879-11099G=	ENSP00000262320.3:n.879-11099G=
ENST00000354866.7:c.879-11099G=	ENSP00000346935.3:n.879-11099G=
ENST00000461023.5:n.176-11099G=
ENST00000481769.1:n.306-11099G=
XM_011522682.1:c.1026-11099G=	XP_011520984.1:n.1026-11099G=
XM_011522682.2:c.1026-11099G=	XP_011520984.1:n.1026-11099G=
XM_011522683.1:c.1026-11099G=	XP_011520985.1:n.1026-11099G=
XM_011522683.2:c.1026-11099G=	XP_011520985.1:n.1026-11099G=
XM_011522684.1:c.879-11099G=	XP_011520986.1:n.879-11099G=
XM_011522684.2:c.879-11099G=	XP_011520986.1:n.879-11099G=
XM_011522685.1:c.63-11099G=	XP_011520987.1:n.63-11099G=
XM_011522687.1:c.63-11099G=	XP_011520989.1:n.63-11099G=
XM_011522688.1:c.-1119-5806G=	XP_011520990.1:n.-1119-5806G=
XM_017023743.1:c.1026-11099G=	XP_016879232.1:n.1026-11099G=
XM_017023744.1:c.1026-11099G=	XP_016879233.1:n.1026-11099G=
XM_017023747.1:c.1026-11099G=	XP_016879236.1:n.1026-11099G=
XM_017023748.1:c.1026-11099G=	XP_016879237.1:n.1026-11099G=
XR_001751996.1:n.1281-11099G=