Canonical Allele Identifier: CA1875198815

Gene: ASTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117375523A= , CM000671.2:g.117375523A=	GRCh38
NC_000009.11:g.120137802A= , CM000671.1:g.120137802A=	GRCh37
NC_000009.10:g.119177623A=	NCBI36
NG_021409.1:g.44516T=
NG_021409.2:g.44535T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313400.9:c.442+38974T= MANE Select	ENSP00000314038.4:n.442+38974T=
ENST00000361477.8:c.442+38974T=	ENSP00000355116.5:n.442+38974T=
ENST00000313400.8:c.442+38974T=	ENSP00000314038.4:n.442+38974T=
ENST00000361209.6:c.442+38974T=	ENSP00000354504.2:n.442+38974T=
ENST00000361477.7:c.-2250+38974T=	ENSP00000355116.4:n.-2250+38974T=
NM_014010.4:c.442+38974T=	NP_054729.3:n.442+38974T=
NM_001365068.1:c.442+38974T= MANE Select	NP_001351997.1:n.442+38974T=
NM_001365069.1:c.442+38974T=	NP_001351998.1:n.442+38974T=
NM_014010.5:c.442+38974T=	NP_054729.3:n.442+38974T=