Canonical Allele Identifier: CA1593493
Community Standard Title: NM_004304.5(ALK):c.4748A>T (p.Asn1583Ile)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29193339T>A , CM000664.2:g.29193339T>A GRCh38
NC_000002.11:g.29416205T>A , CM000664.1:g.29416205T>A GRCh37
NC_000002.10:g.29269709T>A NCBI36
NG_009445.1:g.733228A>T , LRG_488:g.733228A>T

Transcript Alleles

HGVS Amino-acid Change
NM_004304.5:c.4748A>T (ALK) MANE Select NP_004295.2:p.Asn1583Ile
ENST00000389048.8:c.4748A>T (ALK) MANE Select ENSP00000373700.3:p.Asn1583Ile
NM_001353765.1:c.1544A>T (ALK) NP_001340694.1:p.Asn515Ile
NM_001353765.2:c.1544A>T (ALK) NP_001340694.1:p.Asn515Ile
NM_004304.4:c.4748A>T (ALK) NP_004295.2:p.Asn1583Ile
ENST00000389048.7:c.4748A>T (ALK) ENSP00000373700.3:p.Asn1583Ile
ENST00000431873.5:c.1628A>T (ALK) ENSP00000414027.2:p.Asn543Ile
ENST00000431873.6:c.1975A>T (ALK)
ENST00000618119.4:c.3617A>T (ALK) ENSP00000482733.1:p.Asn1206Ile
ENST00000638605.1:n.1625A>T (ALK)
ENST00000642122.1:c.1544A>T (ALK) ENSP00000493203.1:p.Asn515Ile
ENST00000689605.1:c.1923-3589T>A (CLIP4) ENSP00000508948.1:n.1923-3589T>A
XM_024452778.1:c.1901A>T (ALK) XP_024308546.1:p.Asn634Ile
XM_024452779.1:c.1544A>T (ALK) XP_024308547.1:p.Asn515Ile