Canonical Allele Identifier: CA2638710204
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194271A>C , CM000679.2:g.50194271A>C GRCh38
NC_000017.10:g.48271632A>C , CM000679.1:g.48271632A>C GRCh37
NC_000017.9:g.45626631A>C NCBI36
NG_007400.1:g.12369T>G , LRG_1:g.12369T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1614+78T>G MANE Select ENSP00000225964.6:n.1614+78T>G
ENST00000225964.9:c.1614+78T>G ENSP00000225964.5:n.1614+78T>G
ENST00000463440.1:n.4+78T>G
ENST00000471344.1:n.558+78T>G
NM_000088.3:c.1614+78T>G , LRG_1t1:c.1614+78T>G NP_000079.2:n.1614+78T>G
XM_005257058.3:c.1614+78T>G XP_005257115.2:n.1614+78T>G
XM_005257059.3:c.958-1578T>G XP_005257116.2:n.958-1578T>G
XM_011524341.1:c.1416+78T>G XP_011522643.1:n.1416+78T>G
XM_005257058.4:c.1614+78T>G XP_005257115.2:n.1614+78T>G
XM_005257059.4:c.958-1578T>G XP_005257116.2:n.958-1578T>G
NM_000088.4:c.1614+78T>G MANE Select NP_000079.2:n.1614+78T>G