Canonical Allele Identifier: CA2694439366

Gene: COL4A5

Linked Data

• gnomAD v4: X-108568739-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108568739T>C , CM000685.2:g.108568739T>C	GRCh38
NC_000023.10:g.107811969T>C , CM000685.1:g.107811969T>C	GRCh37
NC_000023.9:g.107698625T>C	NCBI36
NG_011977.1:g.133816T>C
NG_011977.2:g.133816T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.322-20T>C MANE Select	ENSP00000331902.7:n.322-20T>C
ENST00000361603.7:c.322-20T>C	ENSP00000354505.2:n.322-20T>C
ENST00000328300.10:c.322-20T>C	ENSP00000331902.6:n.322-20T>C
ENST00000361603.6:c.322-20T>C	ENSP00000354505.2:n.322-20T>C
ENST00000470339.1:n.506-20T>C
NM_000495.4:c.322-20T>C	NP_000486.1:n.322-20T>C
NM_033380.2:c.322-20T>C	NP_203699.1:n.322-20T>C
XM_005262070.2:c.322-20T>C	XP_005262127.1:n.322-20T>C
XM_005262072.3:c.322-20T>C	XP_005262129.1:n.322-20T>C
XM_006724616.2:c.322-20T>C	XP_006724679.1:n.322-20T>C
XM_011530849.1:c.-3-20T>C	XP_011529151.1:n.-3-20T>C
XM_011530850.1:c.322-20T>C	XP_011529152.1:n.322-20T>C
XM_011530849.2:c.337-20T>C	XP_011529151.2:n.337-20T>C
XM_017029259.2:c.337-20T>C	XP_016884748.1:n.337-20T>C
XM_017029260.1:c.337-20T>C	XP_016884749.1:n.337-20T>C
XM_017029261.1:c.337-20T>C	XP_016884750.1:n.337-20T>C
XM_017029262.2:c.337-20T>C	XP_016884751.1:n.337-20T>C
NM_000495.5:c.322-20T>C	NP_000486.1:n.322-20T>C
NM_033380.3:c.322-20T>C MANE Select	NP_203699.1:n.322-20T>C