Canonical Allele Identifier: CA8644744
Community Standard Title: NM_000088.4(COL1A1):c.2608C>T (p.Pro870Ser)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50189864G>A , CM000679.2:g.50189864G>A GRCh38
NC_000017.10:g.48267225G>A , CM000679.1:g.48267225G>A GRCh37
NC_000017.9:g.45622224G>A NCBI36
NG_007400.1:g.16776C>T , LRG_1:g.16776C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2608C>T MANE Select NP_000079.2:p.Pro870Ser
ENST00000225964.10:c.2608C>T MANE Select ENSP00000225964.6:p.Pro870Ser
NM_000088.3:c.2608C>T , LRG_1t1:c.2608C>T NP_000079.2:p.Pro870Ser
ENST00000225964.9:c.2608C>T ENSP00000225964.5:p.Pro870Ser
XM_005257058.3:c.2608C>T XP_005257115.2:p.Pro870Ser
XM_005257058.4:c.2608C>T XP_005257115.2:p.Pro870Ser
XM_005257059.3:c.1690C>T XP_005257116.2:p.Pro564Ser
XM_005257059.4:c.1690C>T XP_005257116.2:p.Pro564Ser
XM_011524341.1:c.2410C>T XP_011522643.1:p.Pro804Ser