Canonical Allele Identifier: CA2501605032

Gene: COL4A5

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108439966_108439968del , CM000685.2:g.108439966_108439968del	GRCh38
NC_000023.10:g.107683196_107683198del , CM000685.1:g.107683196_107683198del	GRCh37
NC_000023.9:g.107569852_107569854del	NCBI36
NG_011977.1:g.5043_5045del
NG_012059.2:g.4514_4516del
NG_011977.2:g.5043_5045del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328300.11:c.-160_-158del MANE Select	ENSP00000331902.7:n.-160_-158del
ENST00000361603.7:c.-160_-158del	ENSP00000354505.2:n.-160_-158del
ENST00000642185.1:c.-160_-158del	ENSP00000495101.1:n.-160_-158del
ENST00000328300.10:c.-160_-158del	ENSP00000331902.6:n.-160_-158del
ENST00000361603.6:c.-160_-158del	ENSP00000354505.2:n.-160_-158del
ENST00000470339.1:n.25_27del
ENST00000477429.1:n.123_125del
NM_000495.4:c.-160_-158del	NP_000486.1:n.-160_-158del
NM_033380.2:c.-160_-158del	NP_203699.1:n.-160_-158del
XM_005262070.2:c.-160_-158del	XP_005262127.1:n.-160_-158del
XM_005262072.3:c.-160_-158del	XP_005262129.1:n.-160_-158del
XM_006724616.2:c.-120-40_-120-38del	XP_006724679.1:n.-120-40_-120-38del
XM_011530850.1:c.-160_-158del	XP_011529152.1:n.-160_-158del
NM_000495.5:c.-160_-158del	NP_000486.1:n.-160_-158del
NM_033380.3:c.-160_-158del MANE Select	NP_203699.1:n.-160_-158del