Canonical Allele Identifier: CA384540774

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48371848G>A (hg19) ; chr12:g.47978065G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47978065G>A , CM000674.2:g.47978065G>A	GRCh38
NC_000012.11:g.48371848G>A , CM000674.1:g.48371848G>A	GRCh37
NC_000012.10:g.46658115G>A	NCBI36
NG_008072.1:g.31438C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.2849C>T	ENSP00000338213.6:p.Pro950Leu
ENST00000380518.8:c.3056C>T MANE Select	ENSP00000369889.3:p.Pro1019Leu
ENST00000337299.6:c.2849C>T	ENSP00000338213.6:p.Pro950Leu
ENST00000380518.7:c.3056C>T	ENSP00000369889.3:p.Pro1019Leu
ENST00000493991.5:n.2142C>T
NM_001844.4:c.3056C>T	NP_001835.3:p.Pro1019Leu
NM_033150.2:c.2849C>T	NP_149162.2:p.Pro950Leu
XM_006719242.2:c.3200C>T	XP_006719305.2:p.Pro1067Leu
XM_011537928.1:c.3200C>T	XP_011536230.1:p.Pro1067Leu
XM_011537929.1:c.3200C>T	XP_011536231.1:p.Pro1067Leu
XM_011537930.1:c.3200C>T	XP_011536232.1:p.Pro1067Leu
XM_011537931.1:c.3200C>T	XP_011536233.1:p.Pro1067Leu
XM_011537932.1:c.3200C>T	XP_011536234.1:p.Pro1067Leu
XM_011537933.1:c.3200C>T	XP_011536235.1:p.Pro1067Leu
XM_011537934.1:c.3197C>T	XP_011536236.1:p.Pro1066Leu
XM_011537935.1:c.2144C>T	XP_011536237.1:p.Pro715Leu
XM_017018828.1:c.3200C>T	XP_016874317.1:p.Pro1067Leu
XM_017018829.1:c.3197C>T	XP_016874318.1:p.Pro1066Leu
XM_017018830.1:c.2990C>T	XP_016874319.1:p.Pro997Leu
XM_017018831.2:c.2510C>T	XP_016874320.1:p.Pro837Leu
NM_001844.5:c.3056C>T MANE Select	NP_001835.3:p.Pro1019Leu
NM_033150.3:c.2849C>T	NP_149162.2:p.Pro950Leu