Canonical Allele Identifier: CA400192005

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263255C>A (hg19) ; chr17:g.50185894C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185894C>A , CM000679.2:g.50185894C>A	GRCh38
NC_000017.10:g.48263255C>A , CM000679.1:g.48263255C>A	GRCh37
NC_000017.9:g.45618254C>A	NCBI36
NG_007400.1:g.20746G>T , LRG_1:g.20746G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4132G>T MANE Select	ENSP00000225964.6:p.Asp1378Tyr
ENST00000225964.9:c.4132G>T	ENSP00000225964.5:p.Asp1378Tyr
ENST00000510710.3:n.1097G>T
NM_000088.3:c.4132G>T , LRG_1t1:c.4132G>T	NP_000079.2:p.Asp1378Tyr
XM_005257058.3:c.3862G>T	XP_005257115.2:p.Asp1288Tyr
XM_005257059.3:c.3214G>T	XP_005257116.2:p.Asp1072Tyr
XM_011524341.1:c.3934G>T	XP_011522643.1:p.Asp1312Tyr
XM_005257058.4:c.3862G>T	XP_005257115.2:p.Asp1288Tyr
XM_005257059.4:c.3214G>T	XP_005257116.2:p.Asp1072Tyr
NM_000088.4:c.4132G>T MANE Select	NP_000079.2:p.Asp1378Tyr