Canonical Allele Identifier: CA1272466283

Gene: ASTL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96130205A= , CM000664.2:g.96130205A=	GRCh38
NC_000002.11:g.96795944A= , CM000664.1:g.96795944A=	GRCh37
NC_000002.10:g.96159671A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342380.3:c.638-60T= MANE Select	ENSP00000343674.2:n.638-60T=
ENST00000342380.2:c.638-60T=	ENSP00000343674.2:n.638-60T=
NM_001002036.3:c.638-60T=	NP_001002036.3:n.638-60T=
XM_011511205.1:c.653-60T=	XP_011509507.1:n.653-60T=
XM_011511206.1:c.641-60T=	XP_011509508.1:n.641-60T=
XM_011511207.1:c.653-60T=	XP_011509509.1:n.653-60T=
XM_011511208.1:c.653-60T=	XP_011509510.1:n.653-60T=
XM_011511205.2:c.653-60T=	XP_011509507.1:n.653-60T=
XM_011511206.2:c.641-60T=	XP_011509508.1:n.641-60T=
XM_011511207.2:c.653-60T=	XP_011509509.1:n.653-60T=
XM_011511208.2:c.653-60T=	XP_011509510.1:n.653-60T=
NM_001002036.4:c.638-60T= MANE Select	NP_001002036.3:n.638-60T=