Canonical Allele Identifier: CA2450634556
Gene: COL4A5 HGNC NCBI

Linked Data

dbSNP Id: rs2064365783

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108439878G>A , CM000685.2:g.108439878G>A GRCh38
NC_000023.10:g.107683108G>A , CM000685.1:g.107683108G>A GRCh37
NC_000023.9:g.107569764G>A NCBI36
NG_011977.1:g.4955G>A
NG_012059.2:g.4597C>T
NG_011977.2:g.4955G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000328300.11:c.-248G>A MANE Select ENSP00000331902.7:n.-248G>A
ENST00000477429.1:n.35G>A
NM_000495.4:c.-248G>A NP_000486.1:n.-248G>A
NM_033380.2:c.-248G>A NP_203699.1:n.-248G>A
XM_005262070.2:c.-248G>A XP_005262127.1:n.-248G>A
XM_005262072.3:c.-248G>A XP_005262129.1:n.-248G>A
XM_006724616.2:c.-121+83G>A XP_006724679.1:n.-121+83G>A
XM_011530850.1:c.-248G>A XP_011529152.1:n.-248G>A
NM_000495.5:c.-248G>A NP_000486.1:n.-248G>A
NM_033380.3:c.-248G>A MANE Select NP_203699.1:n.-248G>A