Canonical Allele Identifier: CA1593831

Gene: ALK

Linked Data

• dbSNP Id: rs759013037
• ExAC: 2:29443537 CACA / C
• gnomAD v2: 2-29443537-CACA-C
• gnomAD v3: 2-29220671-CACA-C
• gnomAD v4: 2-29220671-CACA-C
• MyVariant Identifiers: chr2:g.29443538_29443540del (hg19) ; chr2:g.29220672_29220674del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.29220677_29220679del , CM000664.2:g.29220677_29220679del	GRCh38
NC_000002.11:g.29443543_29443545del , CM000664.1:g.29443543_29443545del	GRCh37
NC_000002.10:g.29297047_29297049del	NCBI36
NG_009445.1:g.705893_705895del , LRG_488:g.705893_705895del

Transcript Alleles

HGVS	Amino-acid change
ENST00000389048.8:c.3645+32_3645+34del MANE Select	ENSP00000373700.3:n.3645+32_3645+34del
ENST00000431873.6:c.872+32_872+34del
ENST00000638605.1:n.522+32_522+34del
ENST00000642122.1:c.441+32_441+34del	ENSP00000493203.1:n.441+32_441+34del
ENST00000389048.7:c.3645+32_3645+34del	ENSP00000373700.3:n.3645+32_3645+34del
ENST00000431873.5:c.525+32_525+34del	ENSP00000414027.2:n.525+32_525+34del
ENST00000618119.4:c.2514+32_2514+34del	ENSP00000482733.1:n.2514+32_2514+34del
NM_004304.4:c.3645+32_3645+34del	NP_004295.2:n.3645+32_3645+34del
NM_001353765.1:c.441+32_441+34del	NP_001340694.1:n.441+32_441+34del
XM_024452778.1:c.798+32_798+34del	XP_024308546.1:n.798+32_798+34del
XM_024452779.1:c.441+32_441+34del	XP_024308547.1:n.441+32_441+34del
NM_004304.5:c.3645+32_3645+34del MANE Select	NP_004295.2:n.3645+32_3645+34del
NM_001353765.2:c.441+32_441+34del	NP_001340694.1:n.441+32_441+34del