Canonical Allele Identifier: CA414132618

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938148G>C (hg19) ; chrX:g.108694918G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108694918G>C , CM000685.2:g.108694918G>C	GRCh38
NC_000023.10:g.107938148G>C , CM000685.1:g.107938148G>C	GRCh37
NC_000023.9:g.107824804G>C	NCBI36
NG_011977.1:g.259995G>C
NG_011977.2:g.259995G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4818G>C MANE Select	ENSP00000331902.7:p.Met1606Ile
ENST00000361603.7:c.4800G>C	ENSP00000354505.2:p.Met1600Ile
ENST00000510690.2:n.1312G>C
ENST00000644079.1:n.1304G>C
ENST00000328300.10:c.4818G>C	ENSP00000331902.6:p.Met1606Ile
ENST00000361603.6:c.4800G>C	ENSP00000354505.2:p.Met1600Ile
ENST00000504541.1:c.216G>C	ENSP00000424845.1:p.Met72Ile
ENST00000515658.1:c.325-1379G>C
NM_000495.4:c.4800G>C	NP_000486.1:p.Met1600Ile
NM_033380.2:c.4818G>C	NP_203699.1:p.Met1606Ile
XM_005262070.2:c.4809G>C	XP_005262127.1:p.Met1603Ile
XM_006724616.2:c.4818G>C	XP_006724679.1:p.Met1606Ile
XM_011530849.1:c.4494G>C	XP_011529151.1:p.Met1498Ile
XM_011530851.1:c.2391G>C	XP_011529153.1:p.Met797Ile
XM_011530849.2:c.4833G>C	XP_011529151.2:p.Met1611Ile
XM_017029259.2:c.4824G>C	XP_016884748.1:p.Met1608Ile
XM_017029260.1:c.4815G>C	XP_016884749.1:p.Met1605Ile
XM_017029263.2:c.3153G>C	XP_016884752.1:p.Met1051Ile
NM_000495.5:c.4800G>C	NP_000486.1:p.Met1600Ile
NM_033380.3:c.4818G>C MANE Select	NP_203699.1:p.Met1606Ile