Canonical Allele Identifier: CA2144064

Gene: COL4A4

Linked Data

• ClinVar Variation Id: 992382
• ClinVar RCV Id: RCV001280823 ; RCV003336370
• dbSNP Id: rs377058706
• ExAC: 2:227872735 A / G
• gnomAD v2: 2-227872735-A-G
• gnomAD v3: 2-227008019-A-G
• gnomAD v4: 2-227008019-A-G
• MyVariant Identifiers: chr2:g.227872735A>G (hg19) ; chr2:g.227008019A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.227008019A>G , CM000664.2:g.227008019A>G	GRCh38
NC_000002.11:g.227872735A>G , CM000664.1:g.227872735A>G	GRCh37
NC_000002.10:g.227580979A>G	NCBI36
NG_011592.1:g.161541T>C , LRG_231:g.161541T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682098.1:c.410T>C	ENSP00000508331.1:p.Met137Thr
ENST00000396625.5:c.4808T>C MANE Select	ENSP00000379866.3:p.Met1603Thr
ENST00000396625.3:c.4808T>C	ENSP00000379866.3:p.Met1603Thr
NM_000092.4:c.4808T>C , LRG_231t1:c.4808T>C	NP_000083.3:p.Met1603Thr
XM_005246281.2:c.4808T>C	XP_005246338.1:p.Met1603Thr
XM_005246282.2:c.4253T>C	XP_005246339.1:p.Met1418Thr
XM_006712246.2:c.4619T>C	XP_006712309.1:p.Met1540Thr
XM_006712249.2:c.4808T>C	XP_006712312.1:p.Met1603Thr
XM_006712252.2:c.4216+14029T>C	XP_006712315.1:n.4216+14029T>C
XM_011510557.1:c.4727T>C	XP_011508859.1:p.Met1576Thr
XM_011510558.1:c.4700T>C	XP_011508860.1:p.Met1567Thr
XM_011510559.1:c.4808T>C	XP_011508861.1:p.Met1603Thr
XM_011510560.1:c.4808T>C	XP_011508862.1:p.Met1603Thr
XM_011510561.1:c.4808T>C	XP_011508863.1:p.Met1603Thr
XM_011510562.1:c.4808T>C	XP_011508864.1:p.Met1603Thr
XM_011510563.1:c.*141T>C	XP_011508865.1:n.*141T>C
XM_011510564.1:c.*141T>C	XP_011508866.1:n.*141T>C
XM_011510565.1:c.4216+14029T>C	XP_011508867.1:n.4216+14029T>C
XM_011510566.1:c.4216+14029T>C	XP_011508868.1:n.4216+14029T>C
XM_011510567.1:c.4216+14029T>C	XP_011508869.1:n.4216+14029T>C
XM_011510569.1:c.4216+14029T>C	XP_011508871.1:n.4216+14029T>C
XM_011510570.1:c.4216+14029T>C	XP_011508872.1:n.4216+14029T>C
XM_011510571.1:c.4216+14029T>C	XP_011508873.1:n.4216+14029T>C
XM_011510572.1:c.3134T>C	XP_011508874.1:p.Met1045Thr
XR_922837.1:n.5118T>C
XR_922838.1:n.5118T>C
XR_922839.1:n.4526+14029T>C
XR_922840.1:n.4526+14029T>C
XM_005246281.3:c.4808T>C	XP_005246338.1:p.Met1603Thr
XM_005246282.3:c.4253T>C	XP_005246339.1:p.Met1418Thr
XM_006712246.3:c.4619T>C	XP_006712309.1:p.Met1540Thr
XM_011510557.2:c.4727T>C	XP_011508859.1:p.Met1576Thr
XM_011510558.2:c.4700T>C	XP_011508860.1:p.Met1567Thr
XM_011510559.2:c.4808T>C	XP_011508861.1:p.Met1603Thr
XM_011510560.2:c.4808T>C	XP_011508862.1:p.Met1603Thr
XM_011510561.2:c.4808T>C	XP_011508863.1:p.Met1603Thr
XM_011510562.2:c.4808T>C	XP_011508864.1:p.Met1603Thr
XM_011510565.2:c.4216+14029T>C	XP_011508867.1:n.4216+14029T>C
XM_011510566.2:c.4216+14029T>C	XP_011508868.1:n.4216+14029T>C
XM_011510567.2:c.4216+14029T>C	XP_011508869.1:n.4216+14029T>C
XM_011510569.2:c.4216+14029T>C	XP_011508871.1:n.4216+14029T>C
XM_011510570.2:c.4216+14029T>C	XP_011508872.1:n.4216+14029T>C
XM_011510572.3:c.3134T>C	XP_011508874.1:p.Met1045Thr
XM_017003296.1:c.4808T>C	XP_016858785.1:p.Met1603Thr
XM_017003297.1:c.4691T>C	XP_016858786.1:p.Met1564Thr
XM_017003298.1:c.4808T>C	XP_016858787.1:p.Met1603Thr
XM_017003300.1:c.4216+14029T>C	XP_016858789.1:n.4216+14029T>C
XR_001738602.1:n.5134T>C
XR_001738603.1:n.5134T>C
XR_001738604.1:n.4880T>C
XR_001738606.1:n.4542+14029T>C
XR_001738607.1:n.4542+14029T>C
XR_922837.2:n.5134T>C
NM_000092.5:c.4808T>C MANE Select	NP_000083.3:p.Met1603Thr