Canonical Allele Identifier: CA346463164

Gene: ALK

Linked Data

• dbSNP Id: rs2148168660
• MyVariant Identifiers: chr2:g.29445247C>G (hg19) ; chr2:g.29222381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29222381C>G , CM000664.2:g.29222381C>G	GRCh38
NC_000002.11:g.29445247C>G , CM000664.1:g.29445247C>G	GRCh37
NC_000002.10:g.29298751C>G	NCBI36
NG_009445.1:g.704186G>C , LRG_488:g.704186G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389048.8:c.3478G>C MANE Select	ENSP00000373700.3:p.Asp1160His
ENST00000431873.6:c.705G>C
ENST00000638605.1:n.355G>C
ENST00000642122.1:c.274G>C	ENSP00000493203.1:p.Asp92His
ENST00000389048.7:c.3478G>C	ENSP00000373700.3:p.Asp1160His
ENST00000431873.5:c.358G>C	ENSP00000414027.2:p.Asp120His
ENST00000453137.1:c.172G>C	ENSP00000387488.1:p.Asp58His
ENST00000618119.4:c.2347G>C	ENSP00000482733.1:p.Asp783His
NM_004304.4:c.3478G>C	NP_004295.2:p.Asp1160His
NM_001353765.1:c.274G>C	NP_001340694.1:p.Asp92His
XM_024452778.1:c.631G>C	XP_024308546.1:p.Asp211His
XM_024452779.1:c.274G>C	XP_024308547.1:p.Asp92His
NM_004304.5:c.3478G>C MANE Select	NP_004295.2:p.Asp1160His
NM_001353765.2:c.274G>C	NP_001340694.1:p.Asp92His