Canonical Allele Identifier: CA400200511

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48265892G>C (hg19) ; chr17:g.50188531G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188531G>C , CM000679.2:g.50188531G>C	GRCh38
NC_000017.10:g.48265892G>C , CM000679.1:g.48265892G>C	GRCh37
NC_000017.9:g.45620891G>C	NCBI36
NG_007400.1:g.18109C>G , LRG_1:g.18109C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3206C>G MANE Select	ENSP00000225964.6:p.Thr1069Ser
ENST00000225964.9:c.3206C>G	ENSP00000225964.5:p.Thr1069Ser
ENST00000486572.1:n.24C>G
ENST00000511732.1:n.150C>G
NM_000088.3:c.3206C>G , LRG_1t1:c.3206C>G	NP_000079.2:p.Thr1069Ser
XM_005257058.3:c.2936C>G	XP_005257115.2:p.Thr979Ser
XM_005257059.3:c.2288C>G	XP_005257116.2:p.Thr763Ser
XM_011524341.1:c.3008C>G	XP_011522643.1:p.Thr1003Ser
XM_005257058.4:c.2936C>G	XP_005257115.2:p.Thr979Ser
XM_005257059.4:c.2288C>G	XP_005257116.2:p.Thr763Ser
NM_000088.4:c.3206C>G MANE Select	NP_000079.2:p.Thr1069Ser