Canonical Allele Identifier: CA411810066

Gene: CYB5R3 A4GALT

Linked Data

• MyVariant Identifiers: chr22:g.43088961G>T (hg19) ; chr22:g.42692955G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42692955G>T , CM000684.2:g.42692955G>T	GRCh38
NC_000022.10:g.43088961G>T , CM000684.1:g.43088961G>T	GRCh37
NC_000022.9:g.41418905G>T	NCBI36
NG_007495.1:g.32916C>A
NG_007495.2:g.33347C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686129.1:c.-49+27842C>A (CYB5R3)	ENSP00000508623.1:n.-49+27842C>A
ENST00000249005.3:c.997C>A (A4GALT)	ENSP00000249005.2:p.Leu333Met
ENST00000381278.4:c.997C>A (A4GALT)	ENSP00000370678.3:p.Leu333Met
ENST00000642412.2:c.997C>A (A4GALT) MANE Select	ENSP00000494127.1:p.Leu333Met
ENST00000249005.2:c.997C>A (A4GALT)	ENSP00000249005.2:p.Leu333Met
ENST00000381278.3:c.997C>A (A4GALT)	ENSP00000370678.3:p.Leu333Met
ENST00000401850.5:c.997C>A (A4GALT)	ENSP00000384794.1:p.Leu333Met
NM_017436.4:c.997C>A (A4GALT)	NP_059132.1:p.Leu333Met
XM_005261643.1:c.997C>A (A4GALT)	XP_005261700.1:p.Leu333Met
XM_005261644.1:c.997C>A (A4GALT)	XP_005261701.1:p.Leu333Met
XM_005261646.3:c.997C>A (A4GALT)	XP_005261703.1:p.Leu333Met
XM_005261647.1:c.997C>A (A4GALT)	XP_005261704.1:p.Leu333Met
XM_005261648.2:c.997C>A (A4GALT)	XP_005261705.1:p.Leu333Met
XM_006724265.2:c.997C>A (A4GALT)	XP_006724328.1:p.Leu333Met
XM_006724266.2:c.997C>A (A4GALT)	XP_006724329.1:p.Leu333Met
XM_011530233.1:c.997C>A (A4GALT)	XP_011528535.1:p.Leu333Met
XM_011530234.1:c.997C>A (A4GALT)	XP_011528536.1:p.Leu333Met
NM_001318038.2:c.997C>A (A4GALT)	NP_001304967.1:p.Leu333Met
NM_017436.6:c.997C>A (A4GALT)	NP_059132.1:p.Leu333Met
XM_005261644.2:c.997C>A (A4GALT)	XP_005261701.1:p.Leu333Met
XM_005261646.4:c.997C>A (A4GALT)	XP_005261703.1:p.Leu333Met
XM_005261647.3:c.997C>A (A4GALT)	XP_005261704.1:p.Leu333Met
XM_005261648.4:c.997C>A (A4GALT)	XP_005261705.1:p.Leu333Met
XM_006724265.3:c.997C>A (A4GALT)	XP_006724328.1:p.Leu333Met
XM_006724266.3:c.997C>A (A4GALT)	XP_006724329.1:p.Leu333Met
XM_011530233.2:c.997C>A (A4GALT)	XP_011528535.1:p.Leu333Met
XM_017028831.1:c.997C>A (A4GALT)	XP_016884320.1:p.Leu333Met
NM_017436.7:c.997C>A (A4GALT) MANE Select	NP_059132.1:p.Leu333Met
NM_001318038.3:c.997C>A (A4GALT)	NP_001304967.1:p.Leu333Met