Canonical Allele Identifier: CA2694415523

Gene: COL4A5

Linked Data

• gnomAD v4: X-108695059-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108695059T>C , CM000685.2:g.108695059T>C	GRCh38
NC_000023.10:g.107938289T>C , CM000685.1:g.107938289T>C	GRCh37
NC_000023.9:g.107824945T>C	NCBI36
NG_011977.1:g.260136T>C
NG_011977.2:g.260136T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.4821+138T>C MANE Select	ENSP00000331902.7:n.4821+138T>C
ENST00000361603.7:c.4803+138T>C	ENSP00000354505.2:n.4803+138T>C
ENST00000510690.2:n.1315+138T>C
ENST00000644079.1:n.1445T>C
ENST00000328300.10:c.4821+138T>C	ENSP00000331902.6:n.4821+138T>C
ENST00000361603.6:c.4803+138T>C	ENSP00000354505.2:n.4803+138T>C
ENST00000504541.1:c.219+138T>C	ENSP00000424845.1:n.219+138T>C
ENST00000515658.1:c.325-1238T>C
NM_000495.4:c.4803+138T>C	NP_000486.1:n.4803+138T>C
NM_033380.2:c.4821+138T>C	NP_203699.1:n.4821+138T>C
XM_005262070.2:c.4812+138T>C	XP_005262127.1:n.4812+138T>C
XM_006724616.2:c.4821+138T>C	XP_006724679.1:n.4821+138T>C
XM_011530849.1:c.4497+138T>C	XP_011529151.1:n.4497+138T>C
XM_011530851.1:c.2394+138T>C	XP_011529153.1:n.2394+138T>C
XM_011530849.2:c.4836+138T>C	XP_011529151.2:n.4836+138T>C
XM_017029259.2:c.4827+138T>C	XP_016884748.1:n.4827+138T>C
XM_017029260.1:c.4818+138T>C	XP_016884749.1:n.4818+138T>C
XM_017029263.2:c.3156+138T>C	XP_016884752.1:n.3156+138T>C
NM_000495.5:c.4803+138T>C	NP_000486.1:n.4803+138T>C
NM_033380.3:c.4821+138T>C MANE Select	NP_203699.1:n.4821+138T>C