Canonical Allele Identifier: CA587805437

Gene: GRHPR

Linked Data

• dbSNP Id: rs1429815494
• gnomAD v2: 9-37436408-TAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC-T
• gnomAD v3: 9-37436411-TAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC-T
• gnomAD v4: 9-37436411-TAGAATACAAATCTTTCATCACATTGTGACTGGGTTTTAGTAGCC-T
• MyVariant Identifiers: chr9:g.37436409_37436452del (hg19) ; chr9:g.37436412_37436455del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37436412_37436455del , CM000671.2:g.37436412_37436455del	GRCh38
NC_000009.11:g.37436409_37436452del , CM000671.1:g.37436409_37436452del	GRCh37
NC_000009.10:g.37426409_37426452del	NCBI36
NG_008135.1:g.18703_18746del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318158.11:c.866-249_866-206del MANE Select	ENSP00000313432.6:n.866-249_866-206del
ENST00000318158.10:c.866-249_866-206del	ENSP00000313432.6:n.866-249_866-206del
ENST00000460882.5:n.893-249_893-206del
ENST00000480596.5:n.1567-249_1567-206del
ENST00000491488.5:n.571-249_571-206del
ENST00000494290.1:c.*52-469_*52-426del	ENSP00000432021.1:n.*52-469_*52-426del
ENST00000497693.1:n.4434-249_4434-206del
NM_012203.1:c.866-249_866-206del	NP_036335.1:n.866-249_866-206del
XM_005251631.1:c.545-249_545-206del	XP_005251688.1:n.545-249_545-206del
XM_011518073.1:c.464-249_464-206del	XP_011516375.1:n.464-249_464-206del
XM_017015320.2:c.946-999_946-956del	XP_016870809.1:n.946-999_946-956del
XM_017015321.2:c.866-999_866-956del	XP_016870810.1:n.866-999_866-956del
XM_017015323.2:c.544-999_544-956del	XP_016870812.1:n.544-999_544-956del
XM_024447716.1:c.1219-999_1219-956del	XP_024303484.1:n.1219-999_1219-956del
XM_024447717.1:c.1139-999_1139-956del	XP_024303485.1:n.1139-999_1139-956del
XR_002956828.1:n.1234-999_1234-956del
XR_002956829.1:n.1154-999_1154-956del
XR_002956830.1:n.2286-249_2286-206del
XR_002956831.1:n.1961-249_1961-206del
XR_002956832.1:n.1285-249_1285-206del
NM_012203.2:c.866-249_866-206del MANE Select	NP_036335.1:n.866-249_866-206del