Canonical Allele Identifier: CA517991648
Gene: COL4A5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107816878A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108573648A>G , CM000685.2:g.108573648A>G GRCh38
NC_000023.10:g.107816878A>G , CM000685.1:g.107816878A>G GRCh37
NC_000023.9:g.107703534A>G NCBI36
NG_011977.1:g.138725A>G
NG_011977.2:g.138725A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000328300.11:c.540A>G MANE Select ENSP00000331902.7:p.Gly180=
ENST00000361603.7:c.540A>G ENSP00000354505.2:p.Gly180=
ENST00000328300.10:c.540A>G ENSP00000331902.6:p.Gly180=
ENST00000361603.6:c.540A>G ENSP00000354505.2:p.Gly180=
NM_000495.4:c.540A>G NP_000486.1:p.Gly180=
NM_033380.2:c.540A>G NP_203699.1:p.Gly180=
XM_005262070.2:c.540A>G XP_005262127.1:p.Gly180=
XM_005262072.3:c.540A>G XP_005262129.1:p.Gly180=
XM_006724616.2:c.540A>G XP_006724679.1:p.Gly180=
XM_011530849.1:c.216A>G XP_011529151.1:p.Gly72=
XM_011530850.1:c.540A>G XP_011529152.1:p.Gly180=
XM_011530849.2:c.555A>G XP_011529151.2:p.Gly185=
XM_017029259.2:c.555A>G XP_016884748.1:p.Gly185=
XM_017029260.1:c.555A>G XP_016884749.1:p.Gly185=
XM_017029261.1:c.555A>G XP_016884750.1:p.Gly185=
XM_017029262.2:c.555A>G XP_016884751.1:p.Gly185=
NM_000495.5:c.540A>G NP_000486.1:p.Gly180=
NM_033380.3:c.540A>G MANE Select NP_203699.1:p.Gly180=