Canonical Allele Identifier: CA1241325258

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29717569T= , CM000664.2:g.29717569T=	GRCh38
NC_000002.11:g.29940435T= , CM000664.1:g.29940435T=	GRCh37
NC_000002.10:g.29793939T=	NCBI36
NG_009445.1:g.208998A= , LRG_488:g.208998A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.787+9A= MANE Select	ENSP00000373700.3:n.787+9A=
ENST00000389048.7:c.787+9A=	ENSP00000373700.3:n.787+9A=
ENST00000618119.4:c.-345+9A=	ENSP00000482733.1:n.-345+9A=
NM_004304.4:c.787+9A=	NP_004295.2:n.787+9A=
XR_001738688.2:n.1717+9A=
NM_004304.5:c.787+9A= MANE Select	NP_004295.2:n.787+9A=