Canonical Allele Identifier: CA291543257
Community Standard Title: NM_000088.4(COL1A1):c.2608C>G (p.Pro870Ala)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2608C>G MANE Select NP_000079.2:p.Pro870Ala
ENST00000225964.10:c.2608C>G MANE Select ENSP00000225964.6:p.Pro870Ala
NM_000088.3:c.2608C>G , LRG_1t1:c.2608C>G NP_000079.2:p.Pro870Ala
ENST00000225964.9:c.2608C>G ENSP00000225964.5:p.Pro870Ala
XM_005257058.3:c.2608C>G XP_005257115.2:p.Pro870Ala
XM_005257058.4:c.2608C>G XP_005257115.2:p.Pro870Ala
XM_005257059.3:c.1690C>G XP_005257116.2:p.Pro564Ala
XM_005257059.4:c.1690C>G XP_005257116.2:p.Pro564Ala
XM_011524341.1:c.2410C>G XP_011522643.1:p.Pro804Ala