Canonical Allele Identifier: CA388664556
Gene: COL4A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.110826999T>C (hg19) chr13:g.110174652T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110174652T>C , CM000675.2:g.110174652T>C GRCh38
NC_000013.10:g.110826999T>C , CM000675.1:g.110826999T>C GRCh37
NC_000013.9:g.109625000T>C NCBI36
NG_011544.2:g.137498A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.3296A>G MANE Select ENSP00000364979.4:p.Lys1099Arg
ENST00000375820.8:c.3296A>G ENSP00000364979.4:p.Lys1099Arg
NM_001845.5:c.3296A>G NP_001836.3:p.Lys1099Arg
XM_011521048.1:c.3104A>G XP_011519350.1:p.Lys1035Arg
XM_011521048.2:c.3104A>G XP_011519350.1:p.Lys1035Arg
NM_001845.6:c.3296A>G MANE Select NP_001836.3:p.Lys1099Arg
Search 100 bp 5'
Search 100 bp 3'