Canonical Allele Identifier: CA484789045

Gene: COL4A1

Linked Data

• MyVariant Identifiers: chr13:g.110864927T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110212580T>G , CM000675.2:g.110212580T>G	GRCh38
NC_000013.10:g.110864927T>G , CM000675.1:g.110864927T>G	GRCh37
NC_000013.9:g.109662928T>G	NCBI36
NG_011544.2:g.99570A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375820.10:c.318A>C MANE Select	ENSP00000364979.4:p.Gly106=
ENST00000543140.6:c.318A>C	ENSP00000443348.1:p.Gly106=
ENST00000615732.2:c.126A>C	ENSP00000478222.2:p.Gly42=
ENST00000647797.1:c.197A>C
ENST00000648170.1:n.197A>C
ENST00000648966.1:c.197A>C
ENST00000649484.1:c.197A>C
ENST00000649738.1:n.448A>C
ENST00000650138.1:n.7A>C
ENST00000375820.8:c.318A>C	ENSP00000364979.4:p.Gly106=
ENST00000543140.5:c.318A>C	ENSP00000443348.1:p.Gly106=
ENST00000615732.1:c.126A>C	ENSP00000478222.1:p.Gly42=
NM_001303110.1:c.318A>C	NP_001290039.1:p.Gly106=
NM_001845.5:c.318A>C	NP_001836.3:p.Gly106=
XM_011521048.1:c.126A>C	XP_011519350.1:p.Gly42=
XM_011521048.2:c.126A>C	XP_011519350.1:p.Gly42=
NM_001845.6:c.318A>C MANE Select	NP_001836.3:p.Gly106=
NM_001303110.2:c.318A>C	NP_001290039.1:p.Gly106=