Canonical Allele Identifier: CA400191857

Gene: COL1A1

Linked Data

• gnomAD v4: 17-50185873-T-G
• MyVariant Identifiers: chr17:g.48263234T>G (hg19) ; chr17:g.50185873T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185873T>G , CM000679.2:g.50185873T>G	GRCh38
NC_000017.10:g.48263234T>G , CM000679.1:g.48263234T>G	GRCh37
NC_000017.9:g.45618233T>G	NCBI36
NG_007400.1:g.20767A>C , LRG_1:g.20767A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4153A>C MANE Select	ENSP00000225964.6:p.Lys1385Gln
ENST00000225964.9:c.4153A>C	ENSP00000225964.5:p.Lys1385Gln
ENST00000510710.3:n.1118A>C
NM_000088.3:c.4153A>C , LRG_1t1:c.4153A>C	NP_000079.2:p.Lys1385Gln
XM_005257058.3:c.3883A>C	XP_005257115.2:p.Lys1295Gln
XM_005257059.3:c.3235A>C	XP_005257116.2:p.Lys1079Gln
XM_011524341.1:c.3955A>C	XP_011522643.1:p.Lys1319Gln
XM_005257058.4:c.3883A>C	XP_005257115.2:p.Lys1295Gln
XM_005257059.4:c.3235A>C	XP_005257116.2:p.Lys1079Gln
NM_000088.4:c.4153A>C MANE Select	NP_000079.2:p.Lys1385Gln