Canonical Allele Identifier: CA484788755
Gene: COL4A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.110822045T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110169698T>C , CM000675.2:g.110169698T>C GRCh38
NC_000013.10:g.110822045T>C , CM000675.1:g.110822045T>C GRCh37
NC_000013.9:g.109620046T>C NCBI36
NG_011544.2:g.142452A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375820.10:c.3807A>G MANE Select ENSP00000364979.4:p.Gly1269=
ENST00000375820.8:c.3807A>G ENSP00000364979.4:p.Gly1269=
NM_001845.5:c.3807A>G NP_001836.3:p.Gly1269=
XM_011521048.1:c.3615A>G XP_011519350.1:p.Gly1205=
XM_011521048.2:c.3615A>G XP_011519350.1:p.Gly1205=
NM_001845.6:c.3807A>G MANE Select NP_001836.3:p.Gly1269=
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Search 100 bp 3'