Canonical Allele Identifier: CA400213772

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48270026C>G (hg19) ; chr17:g.50192665C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50192665C>G , CM000679.2:g.50192665C>G	GRCh38
NC_000017.10:g.48270026C>G , CM000679.1:g.48270026C>G	GRCh37
NC_000017.9:g.45625025C>G	NCBI36
NG_007400.1:g.13975G>C , LRG_1:g.13975G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1904G>C MANE Select	ENSP00000225964.6:p.Gly635Ala
ENST00000225964.9:c.1904G>C	ENSP00000225964.5:p.Gly635Ala
ENST00000476387.1:n.253G>C
NM_000088.3:c.1904G>C , LRG_1t1:c.1904G>C	NP_000079.2:p.Gly635Ala
XM_005257058.3:c.1904G>C	XP_005257115.2:p.Gly635Ala
XM_005257059.3:c.986G>C	XP_005257116.2:p.Gly329Ala
XM_011524341.1:c.1706G>C	XP_011522643.1:p.Gly569Ala
XM_005257058.4:c.1904G>C	XP_005257115.2:p.Gly635Ala
XM_005257059.4:c.986G>C	XP_005257116.2:p.Gly329Ala
NM_000088.4:c.1904G>C MANE Select	NP_000079.2:p.Gly635Ala