Canonical Allele Identifier: CA413851908

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107925002T>G (hg19) ; chrX:g.108681772T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108681772T>G , CM000685.2:g.108681772T>G	GRCh38
NC_000023.10:g.107925002T>G , CM000685.1:g.107925002T>G	GRCh37
NC_000023.9:g.107811658T>G	NCBI36
NG_011977.1:g.246849T>G
NG_011977.2:g.246849T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4100T>G MANE Select	ENSP00000331902.7:p.Leu1367Ter
ENST00000361603.7:c.4082T>G	ENSP00000354505.2:p.Leu1361Ter
ENST00000510690.2:n.594T>G
ENST00000328300.10:c.4100T>G	ENSP00000331902.6:p.Leu1367Ter
ENST00000361603.6:c.4082T>G	ENSP00000354505.2:p.Leu1361Ter
ENST00000489230.1:n.503T>G
NM_000495.4:c.4082T>G	NP_000486.1:p.Leu1361Ter
NM_033380.2:c.4100T>G	NP_203699.1:p.Leu1367Ter
XM_005262070.2:c.4091T>G	XP_005262127.1:p.Leu1364Ter
XM_006724616.2:c.4100T>G	XP_006724679.1:p.Leu1367Ter
XM_011530849.1:c.3776T>G	XP_011529151.1:p.Leu1259Ter
XM_011530851.1:c.1673T>G	XP_011529153.1:p.Leu558Ter
XM_011530849.2:c.4115T>G	XP_011529151.2:p.Leu1372Ter
XM_017029259.2:c.4106T>G	XP_016884748.1:p.Leu1369Ter
XM_017029260.1:c.4097T>G	XP_016884749.1:p.Leu1366Ter
XM_017029263.2:c.2435T>G	XP_016884752.1:p.Leu812Ter
NM_000495.5:c.4082T>G	NP_000486.1:p.Leu1361Ter
NM_033380.3:c.4100T>G MANE Select	NP_203699.1:p.Leu1367Ter