Canonical Allele Identifier: CA1144228973
Community Standard Title: NM_181703.4(GJA5):c.145C= (p.Gln49=)
Gene: GJA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147759094G= , CM000663.2:g.147759094G= GRCh38
NC_000001.10:g.147231202G= , CM000663.1:g.147231202G= GRCh37
NC_000001.9:g.145697826G= NCBI36
NG_009369.2:g.19281C=

Transcript Alleles

HGVS Amino-acid Change
NM_181703.4:c.145C= MANE Select NP_859054.1:p.Gln49=
ENST00000579774.3:c.145C= MANE Select ENSP00000463851.1:p.Gln49=
NM_005266.6:c.145C= NP_005257.2:p.Gln49=
NM_005266.7:c.145C= NP_005257.2:p.Gln49=
NM_181703.3:c.145C= NP_859054.1:p.Gln49=
ENST00000430508.1:c.145C= ENSP00000407645.1:p.Gln49=
ENST00000579774.2:c.145C= ENSP00000463851.1:p.Gln49=
ENST00000621517.1:c.145C= ENSP00000484552.1:p.Gln49=
XM_005272951.3:c.145C= XP_005273008.1:p.Gln49=
XM_005272951.4:c.145C= XP_005273008.1:p.Gln49=
XM_011509415.1:c.145C= XP_011507717.1:p.Gln49=
XM_017001044.1:c.145C= XP_016856533.1:p.Gln49=
XR_922078.1:n.434-18467G=
XR_922079.1:n.434-18467G=
XR_922079.3:n.744-18467G=