Canonical Allele Identifier: CA1874778977

Gene: ASTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116487060C= , CM000671.2:g.116487060C=	GRCh38
NC_000009.11:g.119249339C= , CM000671.1:g.119249339C=	GRCh37
NC_000009.10:g.118289160C=	NCBI36
NG_021409.1:g.932979G=
NG_021409.2:g.932998G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001365068.1:c.3497+299G= MANE Select	NP_001351997.1:n.3497+299G=
ENST00000313400.9:c.3497+299G= MANE Select	ENSP00000314038.4:n.3497+299G=
NM_001184734.1:c.653+299G=	NP_001171663.1:n.653+299G=
NM_001365069.1:c.3485+299G=	NP_001351998.1:n.3485+299G=
NM_014010.4:c.3344+299G=	NP_054729.3:n.3344+299G=
NM_014010.5:c.3344+299G=	NP_054729.3:n.3344+299G=
NM_198186.3:c.800+299G=	NP_937829.3:n.800+299G=
NM_198187.3:c.653+299G=	NP_937830.3:n.653+299G=
NM_198188.2:c.653+299G=	NP_937831.1:n.653+299G=
ENST00000288520.9:c.800+299G=	ENSP00000288520.5:n.800+299G=
ENST00000313400.8:c.3497+299G=	ENSP00000314038.4:n.3497+299G=
ENST00000341734.8:c.653+299G=	ENSP00000339925.4:n.653+299G=
ENST00000361209.6:c.3344+299G=	ENSP00000354504.2:n.3344+299G=
ENST00000361477.7:c.653+299G=	ENSP00000355116.4:n.653+299G=
ENST00000361477.8:c.3344+299G=	ENSP00000355116.5:n.3344+299G=
ENST00000373986.7:c.2666+299G=	ENSP00000363098.3:n.2666+299G=