Canonical Allele Identifier: CA414132885

Gene: COL4A5

Linked Data

• MyVariant Identifiers: chrX:g.107938612A>T (hg19) ; chrX:g.108695382A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695382A>T , CM000685.2:g.108695382A>T	GRCh38
NC_000023.10:g.107938612A>T , CM000685.1:g.107938612A>T	GRCh37
NC_000023.9:g.107825268A>T	NCBI36
NG_011977.1:g.260459A>T
NG_011977.2:g.260459A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.4937A>T MANE Select	ENSP00000331902.7:p.Tyr1646Phe
ENST00000361603.7:c.4919A>T	ENSP00000354505.2:p.Tyr1640Phe
ENST00000510690.2:n.1431A>T
ENST00000644079.1:n.1768A>T
ENST00000328300.10:c.4937A>T	ENSP00000331902.6:p.Tyr1646Phe
ENST00000361603.6:c.4919A>T	ENSP00000354505.2:p.Tyr1640Phe
ENST00000504541.1:c.219+461A>T	ENSP00000424845.1:n.219+461A>T
ENST00000515658.1:c.325-915A>T
NM_000495.4:c.4919A>T	NP_000486.1:p.Tyr1640Phe
NM_033380.2:c.4937A>T	NP_203699.1:p.Tyr1646Phe
XM_005262070.2:c.4928A>T	XP_005262127.1:p.Tyr1643Phe
XM_006724616.2:c.4937A>T	XP_006724679.1:p.Tyr1646Phe
XM_011530849.1:c.4613A>T	XP_011529151.1:p.Tyr1538Phe
XM_011530851.1:c.2510A>T	XP_011529153.1:p.Tyr837Phe
XM_011530849.2:c.4952A>T	XP_011529151.2:p.Tyr1651Phe
XM_017029259.2:c.4943A>T	XP_016884748.1:p.Tyr1648Phe
XM_017029260.1:c.4934A>T	XP_016884749.1:p.Tyr1645Phe
XM_017029263.2:c.3272A>T	XP_016884752.1:p.Tyr1091Phe
NM_000495.5:c.4919A>T	NP_000486.1:p.Tyr1640Phe
NM_033380.3:c.4937A>T MANE Select	NP_203699.1:p.Tyr1646Phe