Canonical Allele Identifier: CA413853732

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107929330A>C (hg19) ; chrX:g.108686100A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108686100A>C , CM000685.2:g.108686100A>C	GRCh38
NC_000023.10:g.107929330A>C , CM000685.1:g.107929330A>C	GRCh37
NC_000023.9:g.107815986A>C	NCBI36
NG_011977.1:g.251177A>C
NG_011977.2:g.251177A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4286A>C MANE Select	ENSP00000331902.7:p.Lys1429Thr
ENST00000361603.7:c.4268A>C	ENSP00000354505.2:p.Lys1423Thr
ENST00000510690.2:n.780A>C
ENST00000328300.10:c.4286A>C	ENSP00000331902.6:p.Lys1429Thr
ENST00000361603.6:c.4268A>C	ENSP00000354505.2:p.Lys1423Thr
ENST00000489230.1:n.689A>C
ENST00000515658.1:c.82A>C
NM_000495.4:c.4268A>C	NP_000486.1:p.Lys1423Thr
NM_033380.2:c.4286A>C	NP_203699.1:p.Lys1429Thr
XM_005262070.2:c.4277A>C	XP_005262127.1:p.Lys1426Thr
XM_006724616.2:c.4286A>C	XP_006724679.1:p.Lys1429Thr
XM_011530849.1:c.3962A>C	XP_011529151.1:p.Lys1321Thr
XM_011530851.1:c.1859A>C	XP_011529153.1:p.Lys620Thr
XM_011530849.2:c.4301A>C	XP_011529151.2:p.Lys1434Thr
XM_017029259.2:c.4292A>C	XP_016884748.1:p.Lys1431Thr
XM_017029260.1:c.4283A>C	XP_016884749.1:p.Lys1428Thr
XM_017029263.2:c.2621A>C	XP_016884752.1:p.Lys874Thr
NM_000495.5:c.4268A>C	NP_000486.1:p.Lys1423Thr
NM_033380.3:c.4286A>C MANE Select	NP_203699.1:p.Lys1429Thr