Canonical Allele Identifier: CA891843688

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107925118_107925119del (hg19) ; chrX:g.108681888_108681889del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108681888_108681889del , CM000685.2:g.108681888_108681889del	GRCh38
NC_000023.10:g.107925118_107925119del , CM000685.1:g.107925118_107925119del	GRCh37
NC_000023.9:g.107811774_107811775del	NCBI36
NG_011977.1:g.246965_246966del
NG_011977.2:g.246965_246966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4216_4216+1del
ENST00000361603.7:c.4198_4198+1del
ENST00000510690.2:n.710_710+1del
ENST00000328300.10:c.4216_4216+1del
ENST00000361603.6:c.4198_4198+1del
ENST00000489230.1:n.619_619+1del
ENST00000515658.1:c.12_12+1del
NM_000495.4:c.4198_4198+1del
NM_033380.2:c.4216_4216+1del
XM_005262070.2:c.4207_4207+1del
XM_006724616.2:c.4216_4216+1del
XM_011530849.1:c.3892_3892+1del
XM_011530851.1:c.1789_1789+1del
XM_011530849.2:c.4231_4231+1del
XM_017029259.2:c.4222_4222+1del
XM_017029260.1:c.4213_4213+1del
XM_017029263.2:c.2551_2551+1del
NM_000495.5:c.4198_4198+1del
NM_033380.3:c.4216_4216+1del