Canonical Allele Identifier: CA13518264

Gene: CD44

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35231725C>T , CM000673.2:g.35231725C>T	GRCh38
NC_000011.9:g.35253272C>T , CM000673.1:g.35253272C>T	GRCh37
NC_000011.8:g.35209848C>T	NCBI36
NG_008937.1:g.97856C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263398.11:c.*2392C>T	ENSP00000263398.6:n.*2392C>T
ENST00000428726.8:c.*2392C>T MANE Select	ENSP00000398632.2:n.*2392C>T
ENST00000263398.10:c.*2392C>T	ENSP00000263398.6:n.*2392C>T
NM_000610.3:c.*2392C>T	NP_000601.3:n.*2392C>T
NM_001001389.1:c.*2392C>T	NP_001001389.1:n.*2392C>T
NM_001001390.1:c.*2392C>T	NP_001001390.1:n.*2392C>T
NM_001001391.1:c.*2392C>T	NP_001001391.1:n.*2392C>T
NM_001001392.1:c.*2438C>T	NP_001001392.1:n.*2438C>T
NM_001202555.1:c.*2392C>T	NP_001189484.1:n.*2392C>T
NM_001202556.1:c.*2392C>T	NP_001189485.1:n.*2392C>T
XM_005253231.2:c.*2392C>T	XP_005253288.1:n.*2392C>T
XM_005253232.2:c.*2392C>T	XP_005253289.1:n.*2392C>T
XM_005253233.2:c.*2392C>T	XP_005253290.1:n.*2392C>T
XM_005253234.2:c.*2392C>T	XP_005253291.1:n.*2392C>T
XM_005253235.2:c.*2392C>T	XP_005253292.1:n.*2392C>T
XM_005253238.2:c.*2392C>T	XP_005253295.1:n.*2392C>T
XM_005253239.2:c.*2392C>T	XP_005253296.1:n.*2392C>T
XM_005253240.2:c.*2392C>T	XP_005253297.1:n.*2392C>T
XM_006718388.1:c.*2392C>T	XP_006718451.1:n.*2392C>T
XM_011520482.1:c.*2392C>T	XP_011518784.1:n.*2392C>T
XM_011520483.1:c.*2392C>T	XP_011518785.1:n.*2392C>T
XM_011520484.1:c.*2392C>T	XP_011518786.1:n.*2392C>T
XM_011520485.1:c.*2392C>T	XP_011518787.1:n.*2392C>T
XM_011520486.1:c.*2392C>T	XP_011518788.1:n.*2392C>T
XM_011520488.1:c.*2392C>T	XP_011518790.1:n.*2392C>T
XM_005253231.3:c.*2392C>T	XP_005253288.1:n.*2392C>T
XM_005253232.3:c.*2392C>T	XP_005253289.1:n.*2392C>T
XM_005253235.3:c.*2392C>T	XP_005253292.1:n.*2392C>T
XM_005253238.3:c.*2392C>T	XP_005253295.1:n.*2392C>T
XM_005253239.3:c.*2392C>T	XP_005253296.1:n.*2392C>T
XM_005253240.3:c.*2392C>T	XP_005253297.1:n.*2392C>T
XM_006718388.2:c.*2392C>T	XP_006718451.1:n.*2392C>T
XM_011520482.2:c.*2392C>T	XP_011518784.1:n.*2392C>T
XM_011520483.2:c.*2392C>T	XP_011518785.1:n.*2392C>T
XM_011520484.2:c.*2392C>T	XP_011518786.1:n.*2392C>T
XM_011520485.2:c.*2392C>T	XP_011518787.1:n.*2392C>T
XM_011520486.2:c.*2392C>T	XP_011518788.1:n.*2392C>T
XM_011520488.2:c.*2392C>T	XP_011518790.1:n.*2392C>T
XM_017018583.2:c.*2392C>T	XP_016874072.1:n.*2392C>T
XM_017018584.2:c.*2392C>T	XP_016874073.1:n.*2392C>T
XM_017018585.2:c.*2392C>T	XP_016874074.1:n.*2392C>T
NM_000610.4:c.*2392C>T MANE Select	NP_000601.3:n.*2392C>T
NM_001001389.2:c.*2392C>T	NP_001001389.1:n.*2392C>T
NM_001001390.2:c.*2392C>T	NP_001001390.1:n.*2392C>T
NM_001001391.2:c.*2392C>T	NP_001001391.1:n.*2392C>T
NM_001001392.2:c.*2438C>T	NP_001001392.1:n.*2438C>T
NM_001202555.2:c.*2392C>T	NP_001189484.1:n.*2392C>T
NM_001202556.2:c.*2392C>T	NP_001189485.1:n.*2392C>T