Canonical Allele Identifier: CA1241144422

Gene: ALK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29328295G= , CM000664.2:g.29328295G=	GRCh38
NC_000002.11:g.29551161G= , CM000664.1:g.29551161G=	GRCh37
NC_000002.10:g.29404665G=	NCBI36
NG_009445.1:g.598272C= , LRG_488:g.598272C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.1414+55C= MANE Select	ENSP00000373700.3:n.1414+55C=
ENST00000389048.7:c.1414+55C=	ENSP00000373700.3:n.1414+55C=
ENST00000618119.4:c.283+55C=	ENSP00000482733.1:n.283+55C=
NM_004304.4:c.1414+55C=	NP_004295.2:n.1414+55C=
XR_939920.1:n.693-90G=
XR_939921.1:n.680+5767G=
XR_001738688.2:n.2344+55C=
XR_244977.4:n.1787G=
XR_939920.2:n.583-90G=
XR_939921.2:n.576+5767G=
XR_939922.2:n.1827G=
NM_004304.5:c.1414+55C= MANE Select	NP_004295.2:n.1414+55C=