Canonical Allele Identifier: CA7047981
Community Standard Title: NM_001845.6(COL4A1):c.1365C>T (p.Gly455=)
Gene: COL4A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110195039G>A , CM000675.2:g.110195039G>A GRCh38
NC_000013.10:g.110847386G>A , CM000675.1:g.110847386G>A GRCh37
NC_000013.9:g.109645387G>A NCBI36
NG_011544.2:g.117111C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001845.6:c.1365C>T MANE Select NP_001836.3:p.Gly455=
ENST00000375820.10:c.1365C>T MANE Select ENSP00000364979.4:p.Gly455=
NM_001303110.1:c.1365C>T NP_001290039.1:p.Gly455=
NM_001303110.2:c.1365C>T NP_001290039.1:p.Gly455=
NM_001845.5:c.1365C>T NP_001836.3:p.Gly455=
ENST00000375820.8:c.1365C>T ENSP00000364979.4:p.Gly455=
ENST00000543140.5:c.1365C>T ENSP00000443348.1:p.Gly455=
ENST00000543140.6:c.1365C>T ENSP00000443348.1:p.Gly455=
ENST00000649738.1:n.1495C>T
XM_011521048.1:c.1173C>T XP_011519350.1:p.Gly391=
XM_011521048.2:c.1173C>T XP_011519350.1:p.Gly391=