Canonical Allele Identifier: CA341162825

Gene: COL11A1

Linked Data

• dbSNP Id: rs1487997708
• MyVariant Identifiers: chr1:g.103444263_103444264del (hg19) ; chr1:g.102978708_102978709del (hg38) ; chr1:g.102978707_102978708del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978709_102978710del , CM000663.2:g.102978709_102978710del	GRCh38
NC_000001.10:g.103444265_103444266del , CM000663.1:g.103444265_103444266del	GRCh37
NC_000001.9:g.103216853_103216854del	NCBI36
NG_008033.1:g.134789_134790del
NG_008033.2:g.134789_134790del

Transcript Alleles

HGVS	Amino-acid change
ENST00000370096.9:c.2754_2754+1del
ENST00000353414.8:c.2637_2637+1del
ENST00000358392.6:c.2790_2790+1del
ENST00000370096.7:c.2754_2754+1del
ENST00000512756.5:c.2406_2406+1del
ENST00000635193.1:c.2088_2088+1del
NM_001190709.1:c.2637_2637+1del
NM_001854.3:c.2754_2754+1del
NM_080629.2:c.2790_2790+1del
NM_080630.3:c.2406_2406+1del
XM_011540719.1:c.2754_2754+1del
XM_011540720.1:c.987_987+1del
XM_011540721.1:c.342_342+1del
XR_946545.1:n.3168_3168+1del
NR_134980.1:n.3088_3088+1del
XM_017000334.1:c.2907_2907+1del
XM_017000335.1:c.2901_2901+1del
XM_017000336.1:c.2907_2907+1del
XM_017000337.1:c.1305_1305+1del
NM_001854.4:c.2754_2754+1del
NM_080630.4:c.2406_2406+1del
NR_134980.2:n.3114_3114+1del
NM_001190709.2:c.2637_2637+1del
NM_080629.3:c.2790_2790+1del