Canonical Allele Identifier: CA425619426

Gene: ALK

Linked Data

• gnomAD v4: 2-29220792-G-A
• MyVariant Identifiers: chr2:g.29443658G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220792G>A , CM000664.2:g.29220792G>A	GRCh38
NC_000002.11:g.29443658G>A , CM000664.1:g.29443658G>A	GRCh37
NC_000002.10:g.29297162G>A	NCBI36
NG_009445.1:g.705775C>T , LRG_488:g.705775C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3559C>T MANE Select	ENSP00000373700.3:p.Leu1187=
ENST00000431873.6:c.786C>T
ENST00000638605.1:n.436C>T
ENST00000642122.1:c.355C>T	ENSP00000493203.1:p.Leu119=
ENST00000389048.7:c.3559C>T	ENSP00000373700.3:p.Leu1187=
ENST00000431873.5:c.439C>T	ENSP00000414027.2:p.Leu147=
ENST00000618119.4:c.2428C>T	ENSP00000482733.1:p.Leu810=
NM_004304.4:c.3559C>T	NP_004295.2:p.Leu1187=
NM_001353765.1:c.355C>T	NP_001340694.1:p.Leu119=
XM_024452778.1:c.712C>T	XP_024308546.1:p.Leu238=
XM_024452779.1:c.355C>T	XP_024308547.1:p.Leu119=
NM_004304.5:c.3559C>T MANE Select	NP_004295.2:p.Leu1187=
NM_001353765.2:c.355C>T	NP_001340694.1:p.Leu119=