Canonical Allele Identifier: CA351140765

Gene: COL4A4

Linked Data

• dbSNP Id: rs1326320251
• gnomAD v2: 2-227872891-A-G
• gnomAD v4: 2-227008175-A-G
• MyVariant Identifiers: chr2:g.227872891A>G (hg19) ; chr2:g.227008175A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227008175A>G , CM000664.2:g.227008175A>G	GRCh38
NC_000002.11:g.227872891A>G , CM000664.1:g.227872891A>G	GRCh37
NC_000002.10:g.227581135A>G	NCBI36
NG_011592.1:g.161385T>C , LRG_231:g.161385T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682098.1:c.254T>C	ENSP00000508331.1:p.Met85Thr
ENST00000396625.5:c.4652T>C MANE Select	ENSP00000379866.3:p.Met1551Thr
ENST00000396625.3:c.4652T>C	ENSP00000379866.3:p.Met1551Thr
NM_000092.4:c.4652T>C , LRG_231t1:c.4652T>C	NP_000083.3:p.Met1551Thr
XM_005246281.2:c.4652T>C	XP_005246338.1:p.Met1551Thr
XM_005246282.2:c.4097T>C	XP_005246339.1:p.Met1366Thr
XM_006712246.2:c.4463T>C	XP_006712309.1:p.Met1488Thr
XM_006712249.2:c.4652T>C	XP_006712312.1:p.Met1551Thr
XM_006712252.2:c.4216+13873T>C	XP_006712315.1:n.4216+13873T>C
XM_011510557.1:c.4571T>C	XP_011508859.1:p.Met1524Thr
XM_011510558.1:c.4544T>C	XP_011508860.1:p.Met1515Thr
XM_011510559.1:c.4652T>C	XP_011508861.1:p.Met1551Thr
XM_011510560.1:c.4652T>C	XP_011508862.1:p.Met1551Thr
XM_011510561.1:c.4652T>C	XP_011508863.1:p.Met1551Thr
XM_011510562.1:c.4652T>C	XP_011508864.1:p.Met1551Thr
XM_011510563.1:c.4398T>C	XP_011508865.1:p.His1466=
XM_011510564.1:c.4281T>C	XP_011508866.1:p.His1427=
XM_011510565.1:c.4216+13873T>C	XP_011508867.1:n.4216+13873T>C
XM_011510566.1:c.4216+13873T>C	XP_011508868.1:n.4216+13873T>C
XM_011510567.1:c.4216+13873T>C	XP_011508869.1:n.4216+13873T>C
XM_011510569.1:c.4216+13873T>C	XP_011508871.1:n.4216+13873T>C
XM_011510570.1:c.4216+13873T>C	XP_011508872.1:n.4216+13873T>C
XM_011510571.1:c.4216+13873T>C	XP_011508873.1:n.4216+13873T>C
XM_011510572.1:c.2978T>C	XP_011508874.1:p.Met993Thr
XR_922837.1:n.4962T>C
XR_922838.1:n.4962T>C
XR_922839.1:n.4526+13873T>C
XR_922840.1:n.4526+13873T>C
XM_005246281.3:c.4652T>C	XP_005246338.1:p.Met1551Thr
XM_005246282.3:c.4097T>C	XP_005246339.1:p.Met1366Thr
XM_006712246.3:c.4463T>C	XP_006712309.1:p.Met1488Thr
XM_011510557.2:c.4571T>C	XP_011508859.1:p.Met1524Thr
XM_011510558.2:c.4544T>C	XP_011508860.1:p.Met1515Thr
XM_011510559.2:c.4652T>C	XP_011508861.1:p.Met1551Thr
XM_011510560.2:c.4652T>C	XP_011508862.1:p.Met1551Thr
XM_011510561.2:c.4652T>C	XP_011508863.1:p.Met1551Thr
XM_011510562.2:c.4652T>C	XP_011508864.1:p.Met1551Thr
XM_011510565.2:c.4216+13873T>C	XP_011508867.1:n.4216+13873T>C
XM_011510566.2:c.4216+13873T>C	XP_011508868.1:n.4216+13873T>C
XM_011510567.2:c.4216+13873T>C	XP_011508869.1:n.4216+13873T>C
XM_011510569.2:c.4216+13873T>C	XP_011508871.1:n.4216+13873T>C
XM_011510570.2:c.4216+13873T>C	XP_011508872.1:n.4216+13873T>C
XM_011510572.3:c.2978T>C	XP_011508874.1:p.Met993Thr
XM_017003296.1:c.4652T>C	XP_016858785.1:p.Met1551Thr
XM_017003297.1:c.4535T>C	XP_016858786.1:p.Met1512Thr
XM_017003298.1:c.4652T>C	XP_016858787.1:p.Met1551Thr
XM_017003300.1:c.4216+13873T>C	XP_016858789.1:n.4216+13873T>C
XR_001738602.1:n.4978T>C
XR_001738603.1:n.4978T>C
XR_001738604.1:n.4724T>C
XR_001738606.1:n.4542+13873T>C
XR_001738607.1:n.4542+13873T>C
XR_922837.2:n.4978T>C
NM_000092.5:c.4652T>C MANE Select	NP_000083.3:p.Met1551Thr