Canonical Allele Identifier: CA363616348
Gene: COL11A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33164400G>C , CM000668.2:g.33164400G>C GRCh38
NC_000006.11:g.33132177G>C , CM000668.1:g.33132177G>C GRCh37
NC_000006.10:g.33240155G>C NCBI36
NG_011589.1:g.33069C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683572.1:n.743C>G
ENST00000341947.7:c.4937C>G MANE Select ENSP00000339915.2:p.Ser1646Ter
ENST00000341947.6:c.4937C>G ENSP00000339915.2:p.Ser1646Ter
ENST00000361917.5:c.4616C>G ENSP00000355123.1:p.Ser1539Ter
ENST00000374708.8:c.4679C>G ENSP00000363840.4:p.Ser1560Ter
ENST00000477772.1:n.727C>G
NM_080679.2:c.4616C>G NP_542410.2:p.Ser1539Ter
NM_080680.2:c.4937C>G NP_542411.2:p.Ser1646Ter
NM_080681.2:c.4679C>G NP_542412.2:p.Ser1560Ter
XM_011514298.1:c.4091C>G XP_011512600.1:p.Ser1364Ter
XM_011514299.1:c.4223C>G XP_011512601.1:p.Ser1408Ter
XM_011514300.1:c.4043C>G XP_011512602.1:p.Ser1348Ter
XM_011514301.1:c.3980C>G XP_011512603.1:p.Ser1327Ter
XM_011514302.1:c.3824C>G XP_011512604.1:p.Ser1275Ter
XM_011514299.2:c.4223C>G XP_011512601.1:p.Ser1408Ter
XM_011514300.2:c.4043C>G XP_011512602.1:p.Ser1348Ter
XM_011514302.2:c.3824C>G XP_011512604.1:p.Ser1275Ter
XM_017010250.1:c.4937C>G XP_016865739.1:p.Ser1646Ter
XM_017010251.2:c.3755C>G XP_016865740.1:p.Ser1252Ter
NM_080680.3:c.4937C>G MANE Select NP_542411.2:p.Ser1646Ter
NM_080681.3:c.4679C>G NP_542412.2:p.Ser1560Ter
NM_080679.3:c.4616C>G NP_542410.2:p.Ser1539Ter