Canonical Allele Identifier: CA414133157

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107939588G>T (hg19) ; chrX:g.108696358G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108696358G>T , CM000685.2:g.108696358G>T	GRCh38
NC_000023.10:g.107939588G>T , CM000685.1:g.107939588G>T	GRCh37
NC_000023.9:g.107826244G>T	NCBI36
NG_011977.1:g.261435G>T
NG_011977.2:g.261435G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.5056G>T MANE Select	ENSP00000331902.7:p.Val1686Leu
ENST00000361603.7:c.5038G>T	ENSP00000354505.2:p.Val1680Leu
ENST00000510690.2:n.1550G>T
ENST00000644079.1:n.2744G>T
ENST00000328300.10:c.5056G>T	ENSP00000331902.6:p.Val1686Leu
ENST00000361603.6:c.5038G>T	ENSP00000354505.2:p.Val1680Leu
ENST00000504541.1:c.281G>T	ENSP00000424845.1:n.281G>T
ENST00000515658.1:c.386G>T
NM_000495.4:c.5038G>T	NP_000486.1:p.Val1680Leu
NM_033380.2:c.5056G>T	NP_203699.1:p.Val1686Leu
XM_005262070.2:c.5047G>T	XP_005262127.1:p.Val1683Leu
XM_006724616.2:c.5056G>T	XP_006724679.1:p.Val1686Leu
XM_011530849.1:c.4732G>T	XP_011529151.1:p.Val1578Leu
XM_011530851.1:c.2629G>T	XP_011529153.1:p.Val877Leu
XM_011530849.2:c.5071G>T	XP_011529151.2:p.Val1691Leu
XM_017029259.2:c.5062G>T	XP_016884748.1:p.Val1688Leu
XM_017029260.1:c.5053G>T	XP_016884749.1:p.Val1685Leu
XM_017029263.2:c.3391G>T	XP_016884752.1:p.Val1131Leu
NM_000495.5:c.5038G>T	NP_000486.1:p.Val1680Leu
NM_033380.3:c.5056G>T MANE Select	NP_203699.1:p.Val1686Leu