Canonical Allele Identifier: CA2263915161
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188489T= , CM000679.2:g.50188489T= GRCh38
NC_000017.10:g.48265850T= , CM000679.1:g.48265850T= GRCh37
NC_000017.9:g.45620849T= NCBI36
NG_007400.1:g.18151A= , LRG_1:g.18151A=

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.3207+41A= MANE Select ENSP00000225964.6:n.3207+41A=
ENST00000225964.9:c.3207+41A= ENSP00000225964.5:n.3207+41A=
ENST00000486572.1:n.66A=
ENST00000511732.1:n.192A=
NM_000088.3:c.3207+41A= , LRG_1t1:c.3207+41A= NP_000079.2:n.3207+41A=
XM_005257058.3:c.2937+41A= XP_005257115.2:n.2937+41A=
XM_005257059.3:c.2289+41A= XP_005257116.2:n.2289+41A=
XM_011524341.1:c.3009+41A= XP_011522643.1:n.3009+41A=
XM_005257058.4:c.2937+41A= XP_005257115.2:n.2937+41A=
XM_005257059.4:c.2289+41A= XP_005257116.2:n.2289+41A=
NM_000088.4:c.3207+41A= MANE Select NP_000079.2:n.3207+41A=