Canonical Allele Identifier: CA349965071

Gene: HECW2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.196319001G>T , CM000664.2:g.196319001G>T	GRCh38
NC_000002.11:g.197183725G>T , CM000664.1:g.197183725G>T	GRCh37
NC_000002.10:g.196891970G>T	NCBI36
NG_053156.1:g.279692C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001348768.2:c.1889C>A MANE Select	NP_001335697.1:p.Thr630Asn
ENST00000644978.2:c.1889C>A MANE Select	ENSP00000495418.1:p.Thr630Asn
NM_001304840.1:c.821C>A	NP_001291769.1:p.Thr274Asn
NM_001304840.2:c.821C>A	NP_001291769.1:p.Thr274Asn
NM_001304840.3:c.821C>A	NP_001291769.1:p.Thr274Asn
NM_001348768.1:c.1889C>A	NP_001335697.1:p.Thr630Asn
NM_020760.2:c.1889C>A	NP_065811.1:p.Thr630Asn
NM_020760.3:c.1889C>A	NP_065811.1:p.Thr630Asn
NM_020760.4:c.1889C>A	NP_065811.1:p.Thr630Asn
ENST00000260983.7:c.1889C>A	ENSP00000260983.2:p.Thr630Asn
ENST00000260983.8:c.1889C>A	ENSP00000260983.2:p.Thr630Asn
ENST00000409111.2:c.821C>A	ENSP00000386775.1:p.Thr274Asn
ENST00000644030.1:c.1910C>A	ENSP00000495504.1:p.Thr637Asn
ENST00000644256.1:c.1889C>A	ENSP00000494649.1:p.Thr630Asn
ENST00000645770.1:n.2101C>A
ENST00000647236.1:c.*1075C>A	ENSP00000494800.1:n.*1075C>A
XM_006712646.2:c.1910C>A	XP_006712709.1:p.Thr637Asn
XM_006712646.3:c.1910C>A	XP_006712709.1:p.Thr637Asn
XM_006712648.2:c.1517C>A	XP_006712711.1:p.Thr506Asn
XM_006712648.4:c.1517C>A	XP_006712711.1:p.Thr506Asn
XM_024453020.1:c.1910C>A	XP_024308788.1:p.Thr637Asn
XM_024453021.1:c.1910C>A	XP_024308789.1:p.Thr637Asn