Canonical Allele Identifier: CA382985826

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118955774G>C (hg19) ; chr11:g.119085064G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119085064G>C , CM000673.2:g.119085064G>C	GRCh38
NC_000011.9:g.118955774G>C , CM000673.1:g.118955774G>C	GRCh37
NC_000011.8:g.118460984G>C	NCBI36
NG_008093.1:g.5188G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442944.7:c.31G>C	ENSP00000392041.3:p.Ala11Pro
ENST00000534956.2:n.34G>C
ENST00000536813.6:c.-104G>C	ENSP00000438726.2:n.-104G>C
ENST00000546302.6:c.31G>C	ENSP00000445599.1:p.Ala11Pro
ENST00000640813.1:c.-21G>C	ENSP00000491061.1:n.-21G>C
ENST00000648026.1:c.25G>C	ENSP00000498044.1:p.Ala9Pro
ENST00000649868.1:c.31G>C	ENSP00000497548.1:p.Ala11Pro
ENST00000652429.1:c.31G>C MANE Select	ENSP00000498786.1:p.Ala11Pro
ENST00000278715.7:c.31G>C	ENSP00000278715.3:p.Ala11Pro
ENST00000442944.6:c.-104G>C	ENSP00000392041.2:n.-104G>C
ENST00000535793.5:c.31G>C	ENSP00000439904.1:p.Ala11Pro
ENST00000536185.5:n.199G>C
ENST00000536813.5:c.31G>C	ENSP00000438726.1:p.Ala11Pro
ENST00000537841.5:c.-112G>C	ENSP00000444730.1:n.-112G>C
ENST00000542044.5:n.156G>C
ENST00000542729.5:c.-112G>C	ENSP00000443058.1:n.-112G>C
ENST00000542822.5:c.31G>C	ENSP00000444817.1:p.Ala11Pro
ENST00000543090.5:c.31G>C	ENSP00000445429.1:p.Ala11Pro
ENST00000543821.5:n.177G>C
ENST00000544387.5:c.31G>C	ENSP00000438424.1:p.Ala11Pro
ENST00000545621.5:c.31G>C	ENSP00000444849.1:p.Ala11Pro
ENST00000545901.5:n.184G>C
ENST00000546302.5:c.31G>C	ENSP00000445599.1:p.Ala11Pro
NM_000190.3:c.31G>C	NP_000181.2:p.Ala11Pro
NM_001258208.1:c.31G>C	NP_001245137.1:p.Ala11Pro
NM_001258209.1:c.-112G>C	NP_001245138.1:n.-112G>C
XM_005271531.1:c.-112G>C	XP_005271588.1:n.-112G>C
XM_005271532.1:c.-88G>C	XP_005271589.1:n.-88G>C
XM_005271533.2:c.31G>C	XP_005271590.1:p.Ala11Pro
NM_000190.4:c.31G>C MANE Select	NP_000181.2:p.Ala11Pro
XM_005271533.3:c.31G>C	XP_005271590.1:p.Ala11Pro
XM_024448460.1:c.31G>C	XP_024304228.1:p.Ala11Pro
NM_001258208.2:c.31G>C	NP_001245137.1:p.Ala11Pro
NM_001258209.2:c.-112G>C	NP_001245138.1:n.-112G>C