Canonical Allele Identifier: CA2638677834
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196936T>G , CM000679.2:g.50196936T>G GRCh38
NC_000017.10:g.48274297T>G , CM000679.1:g.48274297T>G GRCh37
NC_000017.9:g.45629296T>G NCBI36
NG_007400.1:g.9704A>C , LRG_1:g.9704A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.804+74A>C MANE Select ENSP00000225964.6:n.804+74A>C
ENST00000225964.9:c.804+74A>C ENSP00000225964.5:n.804+74A>C
ENST00000495677.1:n.531+74A>C
NM_000088.3:c.804+74A>C , LRG_1t1:c.804+74A>C NP_000079.2:n.804+74A>C
XM_005257058.3:c.804+74A>C XP_005257115.2:n.804+74A>C
XM_005257059.3:c.804+74A>C XP_005257116.2:n.804+74A>C
XM_011524341.1:c.804+74A>C XP_011522643.1:n.804+74A>C
XM_005257058.4:c.804+74A>C XP_005257115.2:n.804+74A>C
XM_005257059.4:c.804+74A>C XP_005257116.2:n.804+74A>C
NM_000088.4:c.804+74A>C MANE Select NP_000079.2:n.804+74A>C