Canonical Allele Identifier: CA413854741

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107930901A>C (hg19) ; chrX:g.108687671A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108687671A>C , CM000685.2:g.108687671A>C	GRCh38
NC_000023.10:g.107930901A>C , CM000685.1:g.107930901A>C	GRCh37
NC_000023.9:g.107817557A>C	NCBI36
NG_011977.1:g.252748A>C
NG_011977.2:g.252748A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4505A>C MANE Select	ENSP00000331902.7:p.Lys1502Thr
ENST00000361603.7:c.4487A>C	ENSP00000354505.2:p.Lys1496Thr
ENST00000510690.2:n.999A>C
ENST00000328300.10:c.4505A>C	ENSP00000331902.6:p.Lys1502Thr
ENST00000361603.6:c.4487A>C	ENSP00000354505.2:p.Lys1496Thr
ENST00000515658.1:c.301A>C
NM_000495.4:c.4487A>C	NP_000486.1:p.Lys1496Thr
NM_033380.2:c.4505A>C	NP_203699.1:p.Lys1502Thr
XM_005262070.2:c.4496A>C	XP_005262127.1:p.Lys1499Thr
XM_006724616.2:c.4505A>C	XP_006724679.1:p.Lys1502Thr
XM_011530849.1:c.4181A>C	XP_011529151.1:p.Lys1394Thr
XM_011530851.1:c.2078A>C	XP_011529153.1:p.Lys693Thr
XM_011530849.2:c.4520A>C	XP_011529151.2:p.Lys1507Thr
XM_017029259.2:c.4511A>C	XP_016884748.1:p.Lys1504Thr
XM_017029260.1:c.4502A>C	XP_016884749.1:p.Lys1501Thr
XM_017029263.2:c.2840A>C	XP_016884752.1:p.Lys947Thr
NM_000495.5:c.4487A>C	NP_000486.1:p.Lys1496Thr
NM_033380.3:c.4505A>C MANE Select	NP_203699.1:p.Lys1502Thr