Canonical Allele Identifier: CA517923395
Gene: COL4A5 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107850040T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108606810T>C , CM000685.2:g.108606810T>C GRCh38
NC_000023.10:g.107850040T>C , CM000685.1:g.107850040T>C GRCh37
NC_000023.9:g.107736696T>C NCBI36
NG_011977.1:g.171887T>C
NG_011977.2:g.171887T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.2313T>C MANE Select ENSP00000331902.7:p.Leu771=
ENST00000361603.7:c.2313T>C ENSP00000354505.2:p.Leu771=
ENST00000328300.10:c.2313T>C ENSP00000331902.6:p.Leu771=
ENST00000361603.6:c.2313T>C ENSP00000354505.2:p.Leu771=
ENST00000483338.1:n.1769T>C
NM_000495.4:c.2313T>C NP_000486.1:p.Leu771=
NM_033380.2:c.2313T>C NP_203699.1:p.Leu771=
XM_005262070.2:c.2313T>C XP_005262127.1:p.Leu771=
XM_005262072.3:c.2313T>C XP_005262129.1:p.Leu771=
XM_006724616.2:c.2313T>C XP_006724679.1:p.Leu771=
XM_011530849.1:c.1989T>C XP_011529151.1:p.Leu663=
XM_011530850.1:c.2313T>C XP_011529152.1:p.Leu771=
XM_011530851.1:c.-33+3749T>C XP_011529153.1:n.-33+3749T>C
XM_011530849.2:c.2328T>C XP_011529151.2:p.Leu776=
XM_017029259.2:c.2328T>C XP_016884748.1:p.Leu776=
XM_017029260.1:c.2328T>C XP_016884749.1:p.Leu776=
XM_017029261.1:c.2328T>C XP_016884750.1:p.Leu776=
XM_017029262.2:c.2328T>C XP_016884751.1:p.Leu776=
XM_017029263.2:c.648T>C XP_016884752.1:p.Leu216=
NM_000495.5:c.2313T>C NP_000486.1:p.Leu771=
NM_033380.3:c.2313T>C MANE Select NP_203699.1:p.Leu771=