Canonical Allele Identifier: CA256274317
Community Standard Title: NM_001845.6(COL4A1):c.43G>A (p.Ala15Thr)
Gene: COL4A1 HGNC NCBI
COL4A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.110306985C>T , CM000675.2:g.110306985C>T GRCh38
NC_000013.10:g.110959332C>T , CM000675.1:g.110959332C>T GRCh37
NC_000013.9:g.109757333C>T NCBI36
NG_011544.2:g.5165G>A
NG_032137.1:g.4702C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001845.6:c.43G>A (COL4A1) MANE Select NP_001836.3:p.Ala15Thr
ENST00000375820.10:c.43G>A (COL4A1) MANE Select ENSP00000364979.4:p.Ala15Thr
NM_001303110.1:c.43G>A (COL4A1) NP_001290039.1:p.Ala15Thr
NM_001303110.2:c.43G>A (COL4A1) NP_001290039.1:p.Ala15Thr
NM_001845.5:c.43G>A (COL4A1) NP_001836.3:p.Ala15Thr
ENST00000375820.8:c.43G>A (COL4A1) ENSP00000364979.4:p.Ala15Thr
ENST00000400163.6:c.-44-875C>T (COL4A2) ENSP00000383027.2:n.-44-875C>T
ENST00000400163.7:c.-44-875C>T (COL4A2) ENSP00000383027.3:n.-44-875C>T
ENST00000543140.5:c.43G>A (COL4A1) ENSP00000443348.1:p.Ala15Thr
ENST00000543140.6:c.43G>A (COL4A1) ENSP00000443348.1:p.Ala15Thr
ENST00000649738.1:n.173G>A (COL4A1)