Canonical Allele Identifier: CA388660688
Gene: COL4A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.110818635G>C (hg19) chr13:g.110166288G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110166288G>C , CM000675.2:g.110166288G>C GRCh38
NC_000013.10:g.110818635G>C , CM000675.1:g.110818635G>C GRCh37
NC_000013.9:g.109616636G>C NCBI36
NG_011544.2:g.145862C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375820.10:c.3965C>G MANE Select ENSP00000364979.4:p.Pro1322Arg
ENST00000650424.1:c.121C>G
ENST00000375820.8:c.3965C>G ENSP00000364979.4:p.Pro1322Arg
NM_001845.5:c.3965C>G NP_001836.3:p.Pro1322Arg
XM_011521048.1:c.3773C>G XP_011519350.1:p.Pro1258Arg
XM_011521048.2:c.3773C>G XP_011519350.1:p.Pro1258Arg
NM_001845.6:c.3965C>G MANE Select NP_001836.3:p.Pro1322Arg
Search 100 bp 5'
Search 100 bp 3'