Canonical Allele Identifier: CA400204108
Community Standard Title: NM_000088.4(COL1A1):c.2974G>A (p.Gly992Ser)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188974C>T , CM000679.2:g.50188974C>T GRCh38
NC_000017.10:g.48266335C>T , CM000679.1:g.48266335C>T GRCh37
NC_000017.9:g.45621334C>T NCBI36
NG_007400.1:g.17666G>A , LRG_1:g.17666G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2974G>A MANE Select NP_000079.2:p.Gly992Ser
ENST00000225964.10:c.2974G>A MANE Select ENSP00000225964.6:p.Gly992Ser
NM_000088.3:c.2974G>A , LRG_1t1:c.2974G>A NP_000079.2:p.Gly992Ser
ENST00000225964.9:c.2974G>A ENSP00000225964.5:p.Gly992Ser
XM_005257058.3:c.2704G>A XP_005257115.2:p.Gly902Ser
XM_005257058.4:c.2704G>A XP_005257115.2:p.Gly902Ser
XM_005257059.3:c.2056G>A XP_005257116.2:p.Gly686Ser
XM_005257059.4:c.2056G>A XP_005257116.2:p.Gly686Ser
XM_011524341.1:c.2776G>A XP_011522643.1:p.Gly926Ser