Canonical Allele Identifier: CA10489422

Gene: COL4A5

Linked Data

• dbSNP Id: rs760241969
• ExAC: X:107938146 A / G
• gnomAD v4: X-108694916-A-G
• MyVariant Identifiers: chrX:g.107938146A>G (hg19) ; chrX:g.108694916A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694916A>G , CM000685.2:g.108694916A>G	GRCh38
NC_000023.10:g.107938146A>G , CM000685.1:g.107938146A>G	GRCh37
NC_000023.9:g.107824802A>G	NCBI36
NG_011977.1:g.259993A>G
NG_011977.2:g.259993A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4816A>G MANE Select	ENSP00000331902.7:p.Met1606Val
ENST00000361603.7:c.4798A>G	ENSP00000354505.2:p.Met1600Val
ENST00000510690.2:n.1310A>G
ENST00000644079.1:n.1302A>G
ENST00000328300.10:c.4816A>G	ENSP00000331902.6:p.Met1606Val
ENST00000361603.6:c.4798A>G	ENSP00000354505.2:p.Met1600Val
ENST00000504541.1:c.214A>G	ENSP00000424845.1:p.Met72Val
ENST00000515658.1:c.325-1381A>G
NM_000495.4:c.4798A>G	NP_000486.1:p.Met1600Val
NM_033380.2:c.4816A>G	NP_203699.1:p.Met1606Val
XM_005262070.2:c.4807A>G	XP_005262127.1:p.Met1603Val
XM_006724616.2:c.4816A>G	XP_006724679.1:p.Met1606Val
XM_011530849.1:c.4492A>G	XP_011529151.1:p.Met1498Val
XM_011530851.1:c.2389A>G	XP_011529153.1:p.Met797Val
XM_011530849.2:c.4831A>G	XP_011529151.2:p.Met1611Val
XM_017029259.2:c.4822A>G	XP_016884748.1:p.Met1608Val
XM_017029260.1:c.4813A>G	XP_016884749.1:p.Met1605Val
XM_017029263.2:c.3151A>G	XP_016884752.1:p.Met1051Val
NM_000495.5:c.4798A>G	NP_000486.1:p.Met1600Val
NM_033380.3:c.4816A>G MANE Select	NP_203699.1:p.Met1606Val