Canonical Allele Identifier: CA400209802
Community Standard Title: NM_000088.4(COL1A1):c.2336G>T (p.Gly779Val)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50190824C>A , CM000679.2:g.50190824C>A GRCh38
NC_000017.10:g.48268185C>A , CM000679.1:g.48268185C>A GRCh37
NC_000017.9:g.45623184C>A NCBI36
NG_007400.1:g.15816G>T , LRG_1:g.15816G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2336G>T MANE Select NP_000079.2:p.Gly779Val
ENST00000225964.10:c.2336G>T MANE Select ENSP00000225964.6:p.Gly779Val
NM_000088.3:c.2336G>T , LRG_1t1:c.2336G>T NP_000079.2:p.Gly779Val
ENST00000225964.9:c.2336G>T ENSP00000225964.5:p.Gly779Val
ENST00000494334.1:n.101G>T
XM_005257058.3:c.2336G>T XP_005257115.2:p.Gly779Val
XM_005257058.4:c.2336G>T XP_005257115.2:p.Gly779Val
XM_005257059.3:c.1418G>T XP_005257116.2:p.Gly473Val
XM_005257059.4:c.1418G>T XP_005257116.2:p.Gly473Val
XM_011524341.1:c.2138G>T XP_011522643.1:p.Gly713Val