Canonical Allele Identifier: CA2695235173

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108440140_108440141del , CM000685.2:g.108440140_108440141del	GRCh38
NC_000023.10:g.107683370_107683371del , CM000685.1:g.107683370_107683371del	GRCh37
NC_000023.9:g.107570026_107570027del	NCBI36
NG_011977.1:g.5217_5218del
NG_012059.2:g.4335_4336del
NG_011977.2:g.5217_5218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.15_16del MANE Select	ENSP00000331902.7:p.Val6GlnfsTer?
ENST00000361603.7:c.15_16del	ENSP00000354505.2:p.Val6GlnfsTer?
ENST00000642185.1:c.15_16del	ENSP00000495101.1:p.Val6GlnfsTer?
ENST00000328300.10:c.15_16del	ENSP00000331902.6:p.Val6GlnfsTer?
ENST00000361603.6:c.15_16del	ENSP00000354505.2:p.Val6GlnfsTer?
ENST00000470339.1:n.199_200del
ENST00000477429.1:n.297_298del
NM_000495.4:c.15_16del	NP_000486.1:p.Val6GlnfsTer?
NM_033380.2:c.15_16del	NP_203699.1:p.Val6GlnfsTer?
XM_005262070.2:c.15_16del	XP_005262127.1:p.Val6GlnfsTer?
XM_005262072.3:c.15_16del	XP_005262129.1:p.Val6GlnfsTer?
XM_006724616.2:c.15_16del	XP_006724679.1:p.Val6GlnfsTer?
XM_011530850.1:c.15_16del	XP_011529152.1:p.Val6GlnfsTer?
NM_000495.5:c.15_16del	NP_000486.1:p.Val6GlnfsTer?
NM_033380.3:c.15_16del MANE Select	NP_203699.1:p.Val6GlnfsTer?