Canonical Allele Identifier: CA2406869979
Gene: CYB5R3 HGNC NCBI
A4GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42692850C= , CM000684.2:g.42692850C= GRCh38
NC_000022.10:g.43088856C= , CM000684.1:g.43088856C= GRCh37
NC_000022.9:g.41418800C= NCBI36
NG_007495.1:g.33021G=
NG_007495.2:g.33452G=

Transcript Alleles

HGVS Amino-acid change
ENST00000686129.1:c.-49+27947G= (CYB5R3) ENSP00000508623.1:n.-49+27947G=
ENST00000249005.3:c.*40G= (A4GALT) ENSP00000249005.2:n.*40G=
ENST00000381278.4:c.*40G= (A4GALT) ENSP00000370678.3:n.*40G=
ENST00000642412.2:c.*40G= (A4GALT) MANE Select ENSP00000494127.1:n.*40G=
ENST00000249005.2:c.*40G= (A4GALT) ENSP00000249005.2:n.*40G=
ENST00000381278.3:c.*40G= (A4GALT) ENSP00000370678.3:n.*40G=
ENST00000401850.5:c.*40G= (A4GALT) ENSP00000384794.1:n.*40G=
NM_017436.4:c.*40G= (A4GALT) NP_059132.1:n.*40G=
XM_005261643.1:c.*40G= (A4GALT) XP_005261700.1:n.*40G=
XM_005261644.1:c.*40G= (A4GALT) XP_005261701.1:n.*40G=
XM_005261646.3:c.*40G= (A4GALT) XP_005261703.1:n.*40G=
XM_005261647.1:c.*40G= (A4GALT) XP_005261704.1:n.*40G=
XM_005261648.2:c.*40G= (A4GALT) XP_005261705.1:n.*40G=
XM_006724265.2:c.*40G= (A4GALT) XP_006724328.1:n.*40G=
XM_006724266.2:c.*40G= (A4GALT) XP_006724329.1:n.*40G=
XM_011530233.1:c.*40G= (A4GALT) XP_011528535.1:n.*40G=
XM_011530234.1:c.*40G= (A4GALT) XP_011528536.1:n.*40G=
NM_001318038.2:c.*40G= (A4GALT) NP_001304967.1:n.*40G=
NM_017436.6:c.*40G= (A4GALT) NP_059132.1:n.*40G=
XM_005261644.2:c.*40G= (A4GALT) XP_005261701.1:n.*40G=
XM_005261646.4:c.*40G= (A4GALT) XP_005261703.1:n.*40G=
XM_005261647.3:c.*40G= (A4GALT) XP_005261704.1:n.*40G=
XM_005261648.4:c.*40G= (A4GALT) XP_005261705.1:n.*40G=
XM_006724265.3:c.*40G= (A4GALT) XP_006724328.1:n.*40G=
XM_006724266.3:c.*40G= (A4GALT) XP_006724329.1:n.*40G=
XM_011530233.2:c.*40G= (A4GALT) XP_011528535.1:n.*40G=
XM_017028831.1:c.*40G= (A4GALT) XP_016884320.1:n.*40G=
NM_017436.7:c.*40G= (A4GALT) MANE Select NP_059132.1:n.*40G=
NM_001318038.3:c.*40G= (A4GALT) NP_001304967.1:n.*40G=