Canonical Allele Identifier: CA362373017

Gene: B4GALT7

Linked Data

• MyVariant Identifiers: chr5:g.177031301G>T (hg19) ; chr5:g.177604300G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177604300G>T , CM000667.2:g.177604300G>T	GRCh38
NC_000005.9:g.177031301G>T , CM000667.1:g.177031301G>T	GRCh37
NC_000005.8:g.176963907G>T	NCBI36
NG_015977.1:g.9183G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000029410.10:c.172G>T MANE Select	ENSP00000029410.5:p.Ala58Ser
ENST00000029410.9:c.172G>T	ENSP00000029410.5:p.Ala58Ser
ENST00000502420.1:n.151G>T
ENST00000505433.5:c.172G>T	ENSP00000425591.1:p.Ala58Ser
ENST00000505468.1:c.-171G>T	ENSP00000420886.1:n.-171G>T
ENST00000510761.1:c.-171G>T	ENSP00000423438.1:n.-171G>T
NM_007255.2:c.172G>T	NP_009186.1:p.Ala58Ser
XM_005265805.2:c.-171G>T	XP_005265862.1:n.-171G>T
XM_006714816.2:c.-328G>T	XP_006714879.1:n.-328G>T
XM_011534421.1:c.-171G>T	XP_011532723.1:n.-171G>T
XM_006714816.4:c.-328G>T	XP_006714879.1:n.-328G>T
XM_017008999.2:c.-171G>T	XP_016864488.1:n.-171G>T
NM_007255.3:c.172G>T MANE Select	NP_009186.1:p.Ala58Ser