Canonical Allele Identifier: CA1315425091
Gene: COL5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189050775_189050776delinsAT , CM000664.2:g.189050775_189050776delinsAT GRCh38
NC_000002.11:g.189915501_189915502delinsAT , CM000664.1:g.189915501_189915502delinsAT GRCh37
NC_000002.10:g.189623746_189623747delinsAT NCBI36
NG_011799.1:g.134104_134105delinsAT
NG_011799.2:g.134104_134105delinsAT
NG_011799.3:g.179526_179527delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.2932-100_2932-99delinsAT MANE Select ENSP00000364000.3:n.2932-100_2932-99delinsAT
ENST00000374866.7:c.2932-100_2932-99delinsAT ENSP00000364000.3:n.2932-100_2932-99delinsAT
ENST00000618828.1:c.1771-100_1771-99delinsAT ENSP00000482184.1:n.1771-100_1771-99delinsAT
NM_000393.3:c.2932-100_2932-99delinsAT NP_000384.2:n.2932-100_2932-99delinsAT
XM_011510573.1:c.2794-100_2794-99delinsAT XP_011508875.1:n.2794-100_2794-99delinsAT
NM_000393.4:c.2932-100_2932-99delinsAT NP_000384.2:n.2932-100_2932-99delinsAT
XM_011510573.3:c.2794-100_2794-99delinsAT XP_011508875.1:n.2794-100_2794-99delinsAT
NM_000393.5:c.2932-100_2932-99delinsAT MANE Select NP_000384.2:n.2932-100_2932-99delinsAT