Canonical Allele Identifier: CA695035505
Gene: COL4A1 HGNC NCBI

Linked Data

dbSNP Id: rs1399160908
gnomAD v3: 13-110174392-C-T
gnomAD v4: 13-110174392-C-T
MyVariant Identifiers: chr13:g.110826739C>T (hg19) chr13:g.110174392C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110174392C>T , CM000675.2:g.110174392C>T GRCh38
NC_000013.10:g.110826739C>T , CM000675.1:g.110826739C>T GRCh37
NC_000013.9:g.109624740C>T NCBI36
NG_011544.2:g.137758G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375820.10:c.3406+54G>A MANE Select ENSP00000364979.4:n.3406+54G>A
ENST00000375820.8:c.3406+54G>A ENSP00000364979.4:n.3406+54G>A
NM_001845.5:c.3406+54G>A NP_001836.3:n.3406+54G>A
XM_011521048.1:c.3214+54G>A XP_011519350.1:n.3214+54G>A
XM_011521048.2:c.3214+54G>A XP_011519350.1:n.3214+54G>A
NM_001845.6:c.3406+54G>A MANE Select NP_001836.3:n.3406+54G>A
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