Canonical Allele Identifier: CA8645270
Community Standard Title: NM_000088.4(COL1A1):c.1360G>A (p.Val454Ile)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194822C>T , CM000679.2:g.50194822C>T GRCh38
NC_000017.10:g.48272183C>T , CM000679.1:g.48272183C>T GRCh37
NC_000017.9:g.45627182C>T NCBI36
NG_007400.1:g.11818G>A , LRG_1:g.11818G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1360G>A MANE Select NP_000079.2:p.Val454Ile
ENST00000225964.10:c.1360G>A MANE Select ENSP00000225964.6:p.Val454Ile
NM_000088.3:c.1360G>A , LRG_1t1:c.1360G>A NP_000079.2:p.Val454Ile
ENST00000225964.9:c.1360G>A ENSP00000225964.5:p.Val454Ile
ENST00000471344.1:n.304G>A
XM_005257058.3:c.1360G>A XP_005257115.2:p.Val454Ile
XM_005257058.4:c.1360G>A XP_005257115.2:p.Val454Ile
XM_005257059.3:c.957+1492G>A XP_005257116.2:n.957+1492G>A
XM_005257059.4:c.957+1492G>A XP_005257116.2:n.957+1492G>A
XM_011524341.1:c.1162G>A XP_011522643.1:p.Val388Ile