Canonical Allele Identifier: CA363616098

Gene: COL11A2

Linked Data

• dbSNP Id: rs1768766989
• gnomAD v4: 6-33164350-G-A
• MyVariant Identifiers: chr6:g.33132127G>A (hg19) ; chr6:g.33164350G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164350G>A , CM000668.2:g.33164350G>A	GRCh38
NC_000006.11:g.33132127G>A , CM000668.1:g.33132127G>A	GRCh37
NC_000006.10:g.33240105G>A	NCBI36
NG_011589.1:g.33119C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.793C>T
ENST00000341947.7:c.4987C>T MANE Select	ENSP00000339915.2:p.Pro1663Ser
ENST00000341947.6:c.4987C>T	ENSP00000339915.2:p.Pro1663Ser
ENST00000361917.5:c.4666C>T	ENSP00000355123.1:p.Pro1556Ser
ENST00000374708.8:c.4729C>T	ENSP00000363840.4:p.Pro1577Ser
ENST00000477772.1:n.777C>T
NM_080679.2:c.4666C>T	NP_542410.2:p.Pro1556Ser
NM_080680.2:c.4987C>T	NP_542411.2:p.Pro1663Ser
NM_080681.2:c.4729C>T	NP_542412.2:p.Pro1577Ser
XM_011514298.1:c.4141C>T	XP_011512600.1:p.Pro1381Ser
XM_011514299.1:c.4273C>T	XP_011512601.1:p.Pro1425Ser
XM_011514300.1:c.4093C>T	XP_011512602.1:p.Pro1365Ser
XM_011514301.1:c.4030C>T	XP_011512603.1:p.Pro1344Ser
XM_011514302.1:c.3874C>T	XP_011512604.1:p.Pro1292Ser
XM_011514299.2:c.4273C>T	XP_011512601.1:p.Pro1425Ser
XM_011514300.2:c.4093C>T	XP_011512602.1:p.Pro1365Ser
XM_011514302.2:c.3874C>T	XP_011512604.1:p.Pro1292Ser
XM_017010250.1:c.4987C>T	XP_016865739.1:p.Pro1663Ser
XM_017010251.2:c.3805C>T	XP_016865740.1:p.Pro1269Ser
NM_080680.3:c.4987C>T MANE Select	NP_542411.2:p.Pro1663Ser
NM_080681.3:c.4729C>T	NP_542412.2:p.Pro1577Ser
NM_080679.3:c.4666C>T	NP_542410.2:p.Pro1556Ser