Canonical Allele Identifier: CA388664532
Gene: COL4A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.110826988C>A (hg19) chr13:g.110174641C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110174641C>A , CM000675.2:g.110174641C>A GRCh38
NC_000013.10:g.110826988C>A , CM000675.1:g.110826988C>A GRCh37
NC_000013.9:g.109624989C>A NCBI36
NG_011544.2:g.137509G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.3307G>T MANE Select ENSP00000364979.4:p.Gly1103Trp
ENST00000375820.8:c.3307G>T ENSP00000364979.4:p.Gly1103Trp
NM_001845.5:c.3307G>T NP_001836.3:p.Gly1103Trp
XM_011521048.1:c.3115G>T XP_011519350.1:p.Gly1039Trp
XM_011521048.2:c.3115G>T XP_011519350.1:p.Gly1039Trp
NM_001845.6:c.3307G>T MANE Select NP_001836.3:p.Gly1103Trp
Search 100 bp 5'
Search 100 bp 3'