Canonical Allele Identifier: CA500848491
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48271361T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194000T>C , CM000679.2:g.50194000T>C GRCh38
NC_000017.10:g.48271361T>C , CM000679.1:g.48271361T>C GRCh37
NC_000017.9:g.45626360T>C NCBI36
NG_007400.1:g.12640A>G , LRG_1:g.12640A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.1710A>G MANE Select ENSP00000225964.6:p.Pro570=
ENST00000225964.9:c.1710A>G ENSP00000225964.5:p.Pro570=
ENST00000463440.1:n.100A>G
ENST00000471344.1:n.742A>G
ENST00000476387.1:n.59A>G
NM_000088.3:c.1710A>G , LRG_1t1:c.1710A>G NP_000079.2:p.Pro570=
XM_005257058.3:c.1710A>G XP_005257115.2:p.Pro570=
XM_005257059.3:c.958-1307A>G XP_005257116.2:n.958-1307A>G
XM_011524341.1:c.1512A>G XP_011522643.1:p.Pro504=
XM_005257058.4:c.1710A>G XP_005257115.2:p.Pro570=
XM_005257059.4:c.958-1307A>G XP_005257116.2:n.958-1307A>G
NM_000088.4:c.1710A>G MANE Select NP_000079.2:p.Pro570=