Canonical Allele Identifier: CA484788698
Gene: COL4A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.110821982G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110169635G>C , CM000675.2:g.110169635G>C GRCh38
NC_000013.10:g.110821982G>C , CM000675.1:g.110821982G>C GRCh37
NC_000013.9:g.109619983G>C NCBI36
NG_011544.2:g.142515C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375820.10:c.3870C>G MANE Select ENSP00000364979.4:p.Gly1290=
ENST00000650424.1:c.26C>G
ENST00000375820.8:c.3870C>G ENSP00000364979.4:p.Gly1290=
NM_001845.5:c.3870C>G NP_001836.3:p.Gly1290=
XM_011521048.1:c.3678C>G XP_011519350.1:p.Gly1226=
XM_011521048.2:c.3678C>G XP_011519350.1:p.Gly1226=
NM_001845.6:c.3870C>G MANE Select NP_001836.3:p.Gly1290=
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