Canonical Allele Identifier: CA2529171699

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108440069T>A , CM000685.2:g.108440069T>A	GRCh38
NC_000023.10:g.107683299T>A , CM000685.1:g.107683299T>A	GRCh37
NC_000023.9:g.107569955T>A	NCBI36
NG_011977.1:g.5146T>A
NG_012059.2:g.4406A>T
NG_011977.2:g.5146T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000328300.11:c.-57T>A MANE Select	ENSP00000331902.7:n.-57T>A
ENST00000361603.7:c.-57T>A	ENSP00000354505.2:n.-57T>A
ENST00000642185.1:c.-57T>A	ENSP00000495101.1:n.-57T>A
ENST00000328300.10:c.-57T>A	ENSP00000331902.6:n.-57T>A
ENST00000361603.6:c.-57T>A	ENSP00000354505.2:n.-57T>A
ENST00000470339.1:n.128T>A
ENST00000477429.1:n.226T>A
NM_000495.4:c.-57T>A	NP_000486.1:n.-57T>A
NM_033380.2:c.-57T>A	NP_203699.1:n.-57T>A
XM_005262070.2:c.-57T>A	XP_005262127.1:n.-57T>A
XM_005262072.3:c.-57T>A	XP_005262129.1:n.-57T>A
XM_006724616.2:c.-57T>A	XP_006724679.1:n.-57T>A
XM_011530850.1:c.-57T>A	XP_011529152.1:n.-57T>A
NM_000495.5:c.-57T>A	NP_000486.1:n.-57T>A
NM_033380.3:c.-57T>A MANE Select	NP_203699.1:n.-57T>A