Canonical Allele Identifier: CA400215635
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194041C>T , CM000679.2:g.50194041C>T GRCh38
NC_000017.10:g.48271402C>T , CM000679.1:g.48271402C>T GRCh37
NC_000017.9:g.45626401C>T NCBI36
NG_007400.1:g.12599G>A , LRG_1:g.12599G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1669G>A MANE Select ENSP00000225964.6:p.Gly557Ser
ENST00000225964.9:c.1669G>A ENSP00000225964.5:p.Gly557Ser
ENST00000463440.1:n.59G>A
ENST00000471344.1:n.701G>A
ENST00000476387.1:n.18G>A
NM_000088.3:c.1669G>A , LRG_1t1:c.1669G>A NP_000079.2:p.Gly557Ser
XM_005257058.3:c.1669G>A XP_005257115.2:p.Gly557Ser
XM_005257059.3:c.958-1348G>A XP_005257116.2:n.958-1348G>A
XM_011524341.1:c.1471G>A XP_011522643.1:p.Gly491Ser
XM_005257058.4:c.1669G>A XP_005257115.2:p.Gly557Ser
XM_005257059.4:c.958-1348G>A XP_005257116.2:n.958-1348G>A
NM_000088.4:c.1669G>A MANE Select NP_000079.2:p.Gly557Ser