Canonical Allele Identifier: CA749813764

Gene: COL6A2

Linked Data

• dbSNP Id: rs1188998811
• MyVariant Identifiers: chr21:g.47545370_47545371insA (hg19) ; chr21:g.46125456_46125457insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46125456_46125457insA , CM000683.2:g.46125456_46125457insA	GRCh38
NC_000021.8:g.47545370_47545371insA , CM000683.1:g.47545370_47545371insA	GRCh37
NC_000021.7:g.46369798_46369799insA	NCBI36
NG_008675.1:g.32338_32339insA , LRG_476:g.32338_32339insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.1817-9_1817-8insA MANE Plus Clinical	ENSP00000380870.1:n.1817-9_1817-8insA
ENST00000300527.9:c.1817-9_1817-8insA MANE Select	ENSP00000300527.4:n.1817-9_1817-8insA
ENST00000409416.6:c.1817-9_1817-8insA	ENSP00000387115.1:n.1817-9_1817-8insA
ENST00000300527.8:c.1817-9_1817-8insA	ENSP00000300527.4:n.1817-9_1817-8insA
ENST00000310645.9:c.1817-9_1817-8insA	ENSP00000312529.5:n.1817-9_1817-8insA
ENST00000397763.5:c.1817-9_1817-8insA	ENSP00000380870.1:n.1817-9_1817-8insA
ENST00000409416.5:c.1817-9_1817-8insA	ENSP00000387115.1:n.1817-9_1817-8insA
ENST00000413758.1:c.479_480insA	ENSP00000395751.1:p.Asp163ArgfsTer3
NM_001849.3:c.1817-9_1817-8insA , LRG_476t1:c.1817-9_1817-8insA	NP_001840.3:n.1817-9_1817-8insA
NM_058174.2:c.1817-9_1817-8insA	NP_478054.2:n.1817-9_1817-8insA
NM_058175.2:c.1817-9_1817-8insA	NP_478055.2:n.1817-9_1817-8insA
XM_011529451.1:c.1817-9_1817-8insA	XP_011527753.1:n.1817-9_1817-8insA
XM_011529452.1:c.1817-9_1817-8insA	XP_011527754.1:n.1817-9_1817-8insA
XR_937438.1:n.1894-9_1894-8insA
XR_937439.1:n.1894-9_1894-8insA
XR_937438.2:n.1901-9_1901-8insA
XR_937439.2:n.1901-9_1901-8insA
NM_001849.4:c.1817-9_1817-8insA MANE Select	NP_001840.3:n.1817-9_1817-8insA
NM_058174.3:c.1817-9_1817-8insA MANE Plus Clinical	NP_478054.2:n.1817-9_1817-8insA
NM_058175.3:c.1817-9_1817-8insA	NP_478055.2:n.1817-9_1817-8insA