Canonical Allele Identifier: CA400221606
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48273680G>T (hg19) chr17:g.50196319G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196319G>T , CM000679.2:g.50196319G>T GRCh38
NC_000017.10:g.48273680G>T , CM000679.1:g.48273680G>T GRCh37
NC_000017.9:g.45628679G>T NCBI36
NG_007400.1:g.10321C>A , LRG_1:g.10321C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.952C>A MANE Select ENSP00000225964.6:p.Pro318Thr
ENST00000225964.9:c.952C>A ENSP00000225964.5:p.Pro318Thr
ENST00000485870.1:n.277C>A
NM_000088.3:c.952C>A , LRG_1t1:c.952C>A NP_000079.2:p.Pro318Thr
XM_005257058.3:c.952C>A XP_005257115.2:p.Pro318Thr
XM_005257059.3:c.952C>A XP_005257116.2:p.Pro318Thr
XM_011524341.1:c.952C>A XP_011522643.1:p.Pro318Thr
XM_005257058.4:c.952C>A XP_005257115.2:p.Pro318Thr
XM_005257059.4:c.952C>A XP_005257116.2:p.Pro318Thr
NM_000088.4:c.952C>A MANE Select NP_000079.2:p.Pro318Thr
Search 100 bp 5'
Search 100 bp 3'